UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
 
FORM 10-Q
 
x
Quarterly Report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934.
 
For the quarterly period ended September 30, 2013
 
¨
Transition Report pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934. 
 
For the transition period from________ to ________
 
Commission File Number:   0-19266
 
ALLIED HEALTHCARE PRODUCTS, INC.
(Exact name of registrant as specified in its charter)
 
Delaware
 
25-1370721
(State or other jurisdiction of
 
(I.R.S. Employer
Incorporation or organization)
 
Identification No.)
 
1720 Sublette Avenue, St. Louis, Missouri 63110
(Address of principal executive offices, including zip code)
 
(314) 771-2400
(Registrant’s telephone number, including area code)
 
N/A
(Former name, former address and former fiscal year, if changed since last report)
 
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding twelve months (or for such shorter periods that the registrant was required to file such reports, and (2) has been subject to such filing requirements for the past ninety days.  Yes  x   No  ¨
 
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).  Yes  x  No ¨
 
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company.  See definitions of "large accelerated filer,” “accelerated filer" and “smaller reporting company” in Rule 12b-2 of the Exchange Act.
 
Large accelerated filer  ¨
Accelerated filer  ¨
 
Non-accelerated filer  ¨
(Do not check if smaller reporting company)
Smaller reporting company  x
 
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).
Yes  ¨  No  x
The number of shares of common stock outstanding at November 4, 2013 is 8,027,147 shares.
 
 
 
INDEX
 
Page
 
 
Number
Part I –
Financial Information
 
 
Item 1.
Financial Statements
                   
 
Statement of Operations -
3
 
Three months ended September 30,
 
 
2013 and 2012 (Unaudited)
 
 
 
Balance Sheet -
4 - 5
 
September 30, 2013 (Unaudited) and
 
 
June 30, 2013
 
 
 
Statement of Cash Flows -
6
 
Three months ended September 30, 2013 and 2012
 
 
(Unaudited)
 
 
 
Notes to Financial Statements
7 – 11
 
 
Item 2.
Management’s Discussion and Analysis of Financial Condition and Results of Operations
12 – 15
 
 
Item 3.
Quantitative and Qualitative Disclosure about Market Risk
15
 
 
Item 4.
Controls and Procedures
15 – 16
 
Part II -
Other Information
 
 
 
 
 
Item 1.
Legal Proceedings
16
 
 
 
 
Item 6.
Exhibits
16 – 17
 
 
 
 
 
 
Signature
18
 
SAFE HARBOR" STATEMENT UNDER THE PRIVATE SECURITIES LITIGATION REFORM ACT OF 1995
 
Statements contained in this Report, which are not historical facts or information, are "forward-looking statements." Words such as "believe," "expect," "intend," "will," "should," and other expressions that indicate future events and trends identify such forward-looking statements. These forward-looking statements involve risks and uncertainties, which could cause the outcome and future results of operations, and financial condition to be materially different than stated or anticipated based on the forward-looking statements. Such risks and uncertainties include both general economic risks and uncertainties, risks and uncertainties affecting the demand for and economic factors affecting the delivery of health care services,  both in the United States and in our overseas markets, impacts of the U.S. Affordable Care Act, the outcome of litigation proceedings and specific matters which relate directly to the Company's operations and properties as discussed in the Company’s annual report on Form 10-K for the year ended June 30, 2013.  The Company cautions that any forward-looking statements contained in this report reflect only the belief of the Company or its management at the time the statement was made. Although the Company believes such forward-looking statements are based upon reasonable assumptions, such assumptions may ultimately prove inaccurate or incomplete. The Company undertakes no obligation to update any forward-looking statement to reflect events or circumstances after the date on which the statement was made.
   
 
2

 
 
PART I.         FINANCIAL INFORMATION
 
Item 1.            Financial Statements
 
ALLIED HEALTHCARE PRODUCTS, INC.
STATEMENT OF OPERATIONS
(UNAUDITED)
 
 
 
Three months ended
 
 
 
September 30,
 
 
 
2013
 
2012
 
 
 
 
 
 
 
 
 
Net sales
 
$
8,708,297
 
$
9,287,091
 
Cost of sales
 
 
6,947,731
 
 
7,308,116
 
Gross profit
 
 
1,760,566
 
 
1,978,975
 
 
 
 
 
 
 
 
 
Selling, general and
 
 
 
 
 
 
 
administrative expenses
 
 
2,622,202
 
 
2,638,575
 
Loss from operations
 
 
(861,636)
 
 
(659,600)
 
 
 
 
 
 
 
 
 
Other (income) expenses:
 
 
 
 
 
 
 
Interest income
 
 
(1,890)
 
 
(4,226)
 
Other, net
 
 
8,723
 
 
7,581
 
 
 
 
6,833
 
 
3,355
 
 
 
 
 
 
 
 
 
Loss before benefit from income taxes
 
 
(868,469)
 
 
(662,955)
 
Benefit from income taxes
 
 
(277,910)
 
 
(251,923)
 
Net loss
 
$
(590,559)
 
$
(411,032)
 
 
 
 
 
 
 
 
 
Basic and diluted loss per share
 
$
(0.07)
 
$
(0.05)
 
 
 
 
 
 
 
 
 
Weighted average shares
outstanding - basic and diluted
 
 
8,027,147
 
 
8,124,386
 
 
See accompanying Notes to Financial Statements.
 
 
3

 
ALLIED HEALTHCARE PRODUCTS, INC.
BALANCE SHEET
ASSETS
 
 
 
(Unaudited)
 
 
 
 
 
 
September 30,
 
June 30,
 
 
 
2013
 
2013
 
 
 
 
 
 
 
 
 
Current assets:
 
 
 
 
 
 
 
Cash and cash equivalents
 
$
3,077,132
 
$
3,687,919
 
Accounts receivable, net of allowances
 
 
 
 
 
 
 
of $170,000
 
 
3,625,782
 
 
4,221,970
 
Inventories, net
 
 
10,245,692
 
 
9,338,343
 
Income tax receivable
 
 
48,520
 
 
36,766
 
Other current assets
 
 
606,946
 
 
420,978
 
Total current assets
 
 
17,604,072
 
 
17,705,976
 
 
 
 
 
 
 
 
 
Property, plant and equipment, net
 
 
9,618,798
 
 
9,722,344
 
Deferred income taxes
 
 
1,943,627
 
 
1,667,699
 
Other assets, net
 
 
228,824
 
 
242,712
 
Total assets
 
$
29,395,321
 
$
29,338,731
 
 
 See accompanying Notes to Financial Statements.
 
(CONTINUED)
 
4

 
ALLIED HEALTHCARE PRODUCTS, INC.
BALANCE SHEET
(CONTINUED)
LIABILITIES AND STOCKHOLDERS' EQUITY
 
 
 
(Unaudited)
 
 
 
 
 
 
September 30,
 
June 30,
 
 
 
2013
 
2013
 
Current liabilities:
 
 
 
 
 
 
 
Accounts payable
 
$
1,695,665
 
$
1,317,202
 
Other accrued liabilities
 
 
2,126,954
 
 
1,861,241
 
Deferred income taxes
 
 
843,557
 
 
845,539
 
Total current liabilities
 
 
4,666,176
 
 
4,023,982
 
 
 
 
 
 
 
 
 
Commitments and contingencies
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stockholders' equity:
 
 
 
 
 
 
 
Preferred stock; $0.01 par value; 1,500,000 shares
    authorized; no shares issued and outstanding
 
 
-
 
 
-
 
Series A preferred stock; $0.01 par value; 200,000 shares
    authorized; no shares issued and outstanding
 
 
-
 
 
-
 
Common stock; $0.01 par value; 30,000,000 shares
    authorized; 10,427,878 shares issued at September 30,
    2013 and June 30, 2013; 8,027,147 shares outstanding
    at September 30, 2013 and June 30, 2013
 
 
104,279
 
 
104,279
 
Additional paid-in capital
 
 
48,589,954
 
 
48,584,999
 
Accumulated deficit
 
 
(2,984,300)
 
 
(2,393,741)
 
Less treasury stock, at cost; 2,400,731 shares at
 
 
 
 
 
 
 
September 30, 2013 and June 30, 2013
 
 
(20,980,788)
 
 
(20,980,788)
 
Total stockholders' equity
 
 
24,729,145
 
 
25,314,749
 
Total liabilities and stockholders' equity
 
$
29,395,321
 
$
29,338,731
 
   
See accompanying Notes to Financial Statements.
 
 
5

 
ALLIED HEALTHCARE PRODUCTS, INC.
STATEMENT OF CASH FLOWS
(UNAUDITED)
 
 
 
Three months ended
 
 
 
September 30,
 
 
 
2013
 
2012
 
 
 
 
 
 
 
 
 
Cash flows from operating activities:
 
 
 
 
 
 
 
Net loss
 
$
(590,559)
 
$
(411,032)
 
Adjustments to reconcile net loss to net
    cash (used in) provided by operating activities:
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Depreciation and amortization
 
 
304,975
 
 
307,346
 
Stock based compensation
 
 
4,955
 
 
11,424
 
Provision for doubtful accounts and sales
 
 
 
 
 
 
 
returns and allowances
 
 
(1,399)
 
 
1,474
 
Deferred taxes
 
 
(277,910)
 
 
(4,569)
 
 
 
 
 
 
 
 
 
Changes in operating assets and liabilities:
 
 
 
 
 
 
 
Accounts receivable
 
 
597,587
 
 
1,138,771
 
Inventories
 
 
(907,349)
 
 
(339,897)
 
Income tax receivable
 
 
(11,754)
 
 
(255,902)
 
Other current assets
 
 
(185,968)
 
 
(257,430)
 
Accounts payable
 
 
378,462
 
 
37,808
 
Deferred revenue
 
 
-
 
 
(114,700)
 
Other accrued liabilities
 
 
265,715
 
 
257,385
 
Net cash (used in) provided by operating activities
 
 
(423,245)
 
 
370,678
 
 
 
 
 
 
 
 
 
Cash flows from investing activities:
 
 
 
 
 
 
 
Capital expenditures
 
 
(187,542)
 
 
(269,161)
 
Net cash used in investing activities
 
 
(187,542)
 
 
(269,161)
 
 
 
 
 
 
 
 
 
Net (decrease) increase in cash and cash equivalents
 
 
(610,787)
 
 
101,517
 
Cash and cash equivalents at beginning of period
 
 
3,687,919
 
 
5,284,543
 
Cash and cash equivalents at end of period
 
$
3,077,132
 
$
5,386,060
 
  
See accompanying Notes to Financial Statements.
 
 
6

 
 ALLIED HEALTHCARE PRODUCTS, INC.
NOTES TO FINANCIAL STATEMENTS
(UNAUDITED)
 
1.  Summary of Significant Accounting and Reporting Policies
 
Basis of Presentation
 
The accompanying unaudited financial statements of Allied Healthcare Products, Inc. (the “Company”) have been prepared in accordance with the instructions for Form 10-Q and do not include all of the information and disclosures required by accounting principles generally accepted in the United States of America for complete financial statements.  In the opinion of management, all adjustments, consisting only of normal recurring adjustments considered necessary for a fair presentation, have been included.  Operating results for any quarter are not necessarily indicative of the results for any other quarter or for the full year.  These statements should be read in conjunction with the financial statements and notes to the financial statements thereto included in the Company’s Annual Report on Form 10-K for the year ended June 30, 2013.

 

Recently Issued Accounting Guidance 
 
We have reviewed accounting guidance and interpretations thereof issued by the FASB, AICPA and the SEC that have effective dates during the periods reported and in future periods. Management does not believe that any of those pronouncements will have a material impact on the Company’s present or future financial statements.   
 
Fair Value of Financial Instruments
 
The Company’s financial instruments consist of cash and cash equivalents, accounts receivable and accounts payable.  The carrying amounts for cash and cash equivalents, accounts receivable and accounts payable approximate their fair value due to the short maturity of these instruments.

2. Inventories
 
Inventories are comprised as follows:
    
 
 
September 30, 2013
 
June 30, 2013
 
 
 
 
 
 
 
 
 
Work-in progress
 
$
679,870
 
$
663,100
 
Component parts
 
 
8,051,900
 
 
7,530,506
 
Finished goods
 
 
2,821,505
 
 
2,457,337
 
Reserve for obsolete and excess inventories
 
 
(1,307,583)
 
 
(1,312,600)
 
 
 
$
10,245,692
 
$
9,338,343
 
 
 
7

 
3.  Earnings per share
 
Basic earnings per share are based on the weighted average number of shares of all common stock outstanding during the period.  Diluted earnings per share are based on the sum of the weighted average number of shares of common stock and common stock equivalents outstanding during the period. The number of basic and diluted shares outstanding for the three months ended September 30, 2013 and 2012 were 8,027,147 and 8,124,386, respectively.

4.  Commitments and Contingencies
 
Legal Claims
 
The Company is subject to various investigations, claims and legal proceedings covering a wide range of matters that arise in the ordinary course of its business activities.  The Company intends to continue to conduct business in such a manner as to avert any FDA action seeking to interrupt or suspend manufacturing or require any recall or modification of products.
 
The Company has recognized the costs and associated liabilities only for those investigations, claims and legal proceedings for which, in its view, it is probable that liabilities have been incurred and the related amounts are estimable.  Based upon information currently available, management believes that existing accrued liabilities are sufficient and that it is not reasonably possible at this time that any additional liabilities will result from the resolution of these matters that would have a material adverse effect on the Company’s results of operations, financial position, or cash flows.
 
Stuyvesant Falls Power Litigation. The Company is currently involved in litigation with Niagara Mohawk Power Corporation d/b/a National Grid (“Niagara”) and other parties, which provides electrical power to the Company’s facility in Stuyvesant Falls, New York.  In fiscal year 2011, Niagara began sending invoices to the Company for electricity used at the Company’s Stuyvesant Falls plant.  The Company maintains in its defense of the lawsuit that it is entitled to a certain amount of free electricity based on covenants running with the land which have been honored for more than a century.  Niagara’s attempts to collect such invoices were stopped in December 2010 by a temporary restraining order, although a court has not yet ruled on the merits of all of Niagara’s claims.  Among other things, Niagara seeks approximately $469,000, which it alleges represents the value of electricity provided prior to the commencement of litigation going back to 2003.  The Company has posted a $250,000 bond which Niagara could draw against for electricity provided and not collected since the December 2010 temporary restraining order in the event Niagara prevails in its lawsuit.  The amount of the bond exceeds the cumulative invoiced electricity charges generated by Niagara since the issuance of the temporary restraining order.  As of September 30, 2013, the Company has not recorded a provision for this matter as management intends to vigorously defend this litigation and believes it is not probable that the Company will be required to pay for electricity as Niagara claims.  The Company believes, however, that any liability it may incur should it not prevail in the litigation would not have a material adverse effect on its financial condition, its result of operations, or its cash flows.
 
 
8

 
Dräger Patent Litigation. On or about October 4, 2013, Dräger Medical GmbH and certain affiliates (the “Dräger Plaintiffs”) filed a patent infringement lawsuit against the Company in the District of Delaware, asserting that the Company infringes United States Patent Nos. 7,487,776 and 8,286,633, both protecting particular combinations of carbon dioxide absorption cartridges and adapters which fit on anesthesia machines. The Dräger Plaintiffs assert that the Company’s sales of certain models of its Litholyme and Carbolyme single-use carbon dioxide absorption cartridges infringe both patents.  The Company has answered the Complaint, asserting invalidity of the patents, non-infringement, and implied license under the doctrine of permissive repair.
 
On October 25, 2013, the Dräger Plaintiffs filed a motion for preliminary injunction requesting that the Company be enjoined from selling certain models of its Litholyme and Carbolyme cartridges during the pendency of the litigation. The Court has set a hearing date of January 17, 2014 on the motion for preliminary injunction.
 
As of September 30, 2013, the Company has not recorded a provision for this matter because the Company cannot estimate a possible loss or range of loss for this matter because the Dräger Plaintiffs have not specified damages claimed and the proceedings are in the early stages.  The Company intends to vigorously contest the motion for preliminary injunction and defend against the litigation brought by the Dräger Plaintiffs and pursue counterclaims for invalidity, non-infringement, and implied license. 
 
Employment Contract
 
The Company has entered into an employment contract with its chief executive officer with annual renewals.  The contract includes termination without cause and change of control provisions, under which the chief executive officer is entitled to receive specified severance payments generally equal to two times ending annual salary if the Company terminates his employment without cause or he voluntarily terminates his employment with “good reason.” “Good Reason” generally includes changes in the scope of his duties or location of employment but also includes (i) the Company’s written election not to renew the Employment Agreement and (ii) certain voluntary resignations by the chief executive officer following a “Change of Control” as defined in the Agreement.
 
9

 
5.  Financing
 
The Company is party to a Loan and Security Agreement, dated November 17, 2009, with Enterprise Bank & Trust (the “Credit Agreement”) pursuant to which the Company obtained a secured revolving credit facility with borrowing availability of up to $5,000,000 (the “Credit Facility”). The Company’s obligations under the Credit Facility are secured by certain assets of the Company pursuant to the terms and subject to the conditions set forth in the Credit Agreement.
 
The Credit Facility was amended on November 12, 2013 extending the maturity date to November 11, 2014. The Credit Facility will be available on a revolving basis until it expires on November 11, 2014, at which time all amounts outstanding under the Credit Facility will be due and payable. Advances under the Credit Facility will be made pursuant to a Revolving Credit Note executed by the Company in favor of Enterprise Bank & Trust. Such advances will bear interest at a rate equal to 3.50% in excess of the 30-day LIBOR rate.  Advances may be prepaid in whole or in part without premium or penalty.   
 
Under the Credit Agreement, advances are generally subject to customary borrowing conditions. The Credit Agreement also contains covenants with which the Company must comply during the term of the Credit Facility. Among other things, such covenants restrict the Company’s ability to incur certain additional debt; make specified restricted payments, dividends and capital expenditures; authorize or issue capital stock; enter into certain transactions with affiliates; consolidate or merge with or acquire another business; sell certain of its assets or dissolve or wind up the Company. The Credit Agreement also contains certain events of default that are customary for financings of this type including, without limitation: the failure to pay principal, interest, fees or other amounts when due; the breach of specified representations or warranties contained in the loan documents; cross-default with certain other indebtedness of the Company; the entry of uninsured judgments that are not bonded or stayed; failure to comply with the observance or performance of specified agreements contained in the loan documents; commencement of bankruptcy or other insolvency proceedings; and the failure of any of the loan documents entered into in connection with the Credit Facility to be in full force and effect. After an event of default, and upon the continuation thereof, the principal amount of all loans made under the Credit Facility would bear interest at a rate per annum equal to 4.00% above the otherwise applicable interest rate (provided, that the interest rate may not exceed the highest rate permissible under law), and the lender would have the option to accelerate maturity and payment of the Company’s obligations under the Credit Facility.
 
The 30-day LIBOR rate was 0.18% on September 30, 2013.
 
At September 30, 2013 the Company had no aggregate indebtedness, including capital lease obligations, short-term debt and long term debt.
 
The Company was in compliance with all of the covenants associated with the Credit Facility at September 30, 2013.
 
10

 
6.  Baralyme® Agreement
 
A reconciliation of deferred revenue resulting from the agreement with Abbott Laboratories (“Abbott”), with the amounts received under the agreement, and amounts recognized as net sales is as follows: 
 
 
 
Three Months ended
 
 
 
September 30,
 
 
 
2013
 
2012
 
 
 
 
 
 
 
 
 
Beginning balance
 
$
                   -
 
$
114,700
 
 
 
 
 
 
 
 
 
Revenue recognized
as net sales
 
 
-
 
 
(114,700)
 
 
 
 
-
 
 
-
 
 
 
 
 
 
 
 
 
Less - Current portion
of deferred revenue
 
 
-
 
 
-
 
 
 
$
-
 
$
-
 

7.  Share Repurchases
 
On November 21, 2012 the Company’s Board of Directors approved the purchase of up to 100,000 shares of the Company’s common stock.  This authority terminated on February 19th, 2013.  Pursuant to this authorization, the Company repurchased 94,139 shares of stock at an average price of $2.54 for an aggregate total purchase price of $240,952. 
 
On February 25, 2013 the Company’s Board of Directors authorized the repurchase of up to 100,000 shares of the Company’s common stock for a period of 90 days.  Repurchases may be made in the open market or in privately negotiated transactions, with the timing and terms of such transaction in the discretion of the Chairman of the Board unless terminated by the Board, the repurchase authority renews for successive 90 day periods.  The repurchase authority may be terminated by the Board at any time and without notice.  Pursuant to this authorization, the Company repurchased a total of 3,100 shares in the third quarter of fiscal  2013 at an average price of $2.69 per share for an aggregate total purchase price of $8,408.

8.  Income Taxes
 
The Company accounts for income taxes under ASC Topic 740: “Income Taxes.” Under ASC 740, the deferred tax provision is determined using the liability method, whereby deferred tax assets and liabilities are recognized based upon temporary differences between the financial statement and income tax bases of assets and liabilities using presently enacted tax rates. Valuation allowances are established when necessary to reduce deferred tax assets to the amounts expected to be realized.  The company has relied on the reversal of existing temporary deferred tax liabilities and tax planning strategies to support the value of its deferred tax assets.  In the quarter ended September 30, 2013 the company’s cumulative losses have exceeded the value available through those strategies and a valuation allowance of approximately $31,000 has been established. To the extent that the Company’s losses continue in future quarters, the tax benefit of those losses would be subject to a valuation allowance.
 
 
11

 
Item 2.  Management’s Discussion and Analysis of Financial Conditions and Results of Operations
 
Three months ended September 30, 2013 compared to three months ended September 30, 2012
 
Allied had net sales of $8.7 million for the three months ended September 30, 2013, down $0.6 million from net sales of $9.3 million in the prior year same quarter. Domestic sales were down 6.2% while international sales, which represented 22.8% of first quarter sales, were down 6.3% from the prior year same quarter.
 
Sales for the three months ended September 30, 2013 and 2012 included $-, and  $114,700, respectively, for the recognition of income from payments resulting from the agreement with Abbott Laboratories to cease the production and distribution of Baralyme®.  Income from the agreement was recognized at $57,350 per month until the expiration of the agreement in August 2012.  Allied continues to sell Carbolime®, a carbon dioxide absorbent with a different formulation than Baralyme®, as well as Litholyme®, a new premium carbon dioxide absorbent. The Company ceased the sale of Baralyme® on August 27, 2004.   
  
Orders for the Company’s products for the three months ended September 30, 2013 of $8.8 million were $0.8 million or 8.3% lower than orders for the prior year same quarter of $9.6 million.  Domestic orders are down 2.9% over the prior year same quarter while international orders, which represented 24.2% of first quarter orders, were 20.8% lower than orders for the prior year same quarter. The Company continues to believe that the purchase of equipment and durable goods and the purchase of equipment by hospitals and municipalities have been cut to meet budgets and conserve cash due to the slow recovery of the economy since the recession in 2008. Orders and sales remain below pre-recession levels. The Company also believes domestic markets are further negatively impacted by uncertainty from the implementation of the Affordable Care Act.  The Company believes that the decrease in international orders and sales reflects fluctuation in international demand and order levels, and a reduction in governmental medical expenditures in several countries including Venezuela.  The Company does not believe this decrease indicates a drop in market share.
 
Gross profit for the three months ended September 30, 2013 was $1.8 million, or 20.7% of net sales, compared to $2.0 million, or 21.5% of net sales, for the three months ended September 30, 2012. Gross profit, as a percentage of sales, was negatively impacted by the $114,700 reduction in payments resulting from the Abbott agreement recognized in sales and income.  In addition, lower sales have led to lower utilization of fixed expenses in the Company’s manufacturing operations.   Gross profit for the three months ended September 30, 2013 was also negatively impacted by approximately $72,000 as a result of the Medical Device Excise Tax.  Under the U.S. Affordable Care Act, beginning on January 1, 2013, the excise tax is imposed on all U.S. sales of certain medical devices.  The tax is 2.3% of the selling price of the taxable product, subject to certain exceptions.
 
 
12

 
Selling, general and administrative expenses for the three months ended September 30, 2013 were $2.6 million unchanged from the same quarter a year ago.  Legal expenses were approximately $36,000 higher than in the prior year and recruiting expenses were approximately $16,000 higher than in the prior year. These increases have been offset by a decrease in other expense accounts including a $30,000 decrease in audit expenses, and an approximately $29,000 decrease in outside engineering consulting charges.
 
               Loss from operations was $861,636 for the three months ended September 30, 2013 compared to loss from operations of $659,600 for the three months ended September 30, 2012.
 
               Allied had a loss before benefit from income taxes in the first quarter of fiscal 2014 of $868,469 compared to a loss before benefit from income taxes in the first quarter of fiscal 2013 of $662,955.  The Company recorded a tax benefit of $277,910 for the three months ended September 30, 2013 compared to a tax benefit of $251,923 for the three months ended September 30, 2012. As previously disclosed in the Company’s annual report on Form 10-K for the 2013 fiscal year, the Company’s deferred tax assets has been based on the reversal of existing temporary deferred tax liabilities and tax planning strategies. In the quarter ended September 30, 2013 the Company’s cumulative losses have exceeded the value of the deferred tax assets and a valuation allowance of approximately $31,000 has been established. To the extent that the Company’s losses continue in future quarters, the tax benefit of those losses would be reduced by a valuation allowance.
 
Net loss for the first quarter of fiscal 2014 was $590,559 or $0.07 per basic and diluted share compared to net loss of $411,032 or $0.05 per basic and diluted share for the first quarter of fiscal 2013.  The weighted average number of common shares outstanding, used in the calculation of basic and diluted earnings per share for the first quarters of fiscal 2014 and 2013 were 8,027,147 and 8,124,386, respectively. 
   

Liquidity and Capital Resources

 
The Company believes that available resources, including availability under a credit facility described below, are sufficient to meet operating requirements in the coming year.
 
 
13

 
The Company’s working capital was $12.9 million at September 30, 2013 compared to $13.7 million at June 30, 2013.  The decrease in working capital was primarily a result of accounts receivable which decreased by $0.6 million largely due to a decrease in sales.  Accounts receivable as measured in days of sales outstanding (“DSO”) was 40 DSO at September 30, 2013; up from 39 DSO at June 30, 2013.  Accounts Payable increased by approximately $0.4 million, and Accrued Liabilities increased by approximately $0.3 million, primarily as a result of the timing of payrolls.   In addition cash and cash equivalents decreased by $0.6 million.  At September 30, 2013 these decreases in working capital were offset by an increase in inventory of $0.9 million and an increase in other current assets of $0.2 million.  The increase in other current assets is a result of prepayment of the Company’s insurance premiums for the fiscal year.
 
The Company is party to a Loan and Security Agreement, dated November 17, 2009, with Enterprise Bank & Trust (the “Credit Agreement”) pursuant to which the Company has a secured revolving credit facility with borrowing availability of up to $5,000,000 (the “Credit Facility”). The Company’s obligations under the Credit Facility are secured by certain assets of the Company pursuant to the terms and subject to the conditions set forth in the Credit Agreement.  See Note 5 – Financing to the Company’s unaudited financial statements for more information concerning the Credit Facility. 
 
Advances under the Credit Facility will be made pursuant to a Revolving Credit Note executed by the Company in favor of Enterprise Bank & Trust. Such advances will bear interest at a rate equal to the 30-day LIBOR rate plus 3.50%.  Advances may be prepaid in whole or in part without premium or penalty.  The 30-day LIBOR rate was 0.18% on September 30, 2013.
 
At September 30, 2013 the Company had no aggregate indebtedness, including capital lease obligations, short-term debt and long term debt.
 
In the event that economic conditions were to severely worsen for a protracted period of time, we believe that we will have borrowing capacity under credit facilities that will provide sufficient financial flexibility.  The Company would have options available, including postponing capital expenditures, to ensure liquidity in addition to increased borrowing.
 
Inflation has not had a material effect on the Company’s business or results of operations during the first quarter of fiscal 2014. 
 
Litigation and Contingencies 
 
The Company becomes, from time to time, a party to personal injury litigation arising out of incidents involving the use of its products. The Company believes that any potential judgments resulting from these claims over its self-insured retention will be covered by the Company’s product liability insurance.  The Company is also currently a defendant in a patent infringement claim brought by Dräger Medical GmbH and its affiliates related to certain models of the Company’s Litholyme and Carbolyme single-use carbon dioxide absorption cartridges. See Part II, Item 1 – Legal Proceedings, below, for more information concerning litigation.
 
 
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Critical Accounting Policies

 

The impact and any associated risks related to the Company’s critical accounting policies on business operations are discussed throughout “Management’s Discussion and Analysis of Financial Condition and Results of Operations,” where such policies affect the Company’s reported and expected financial results. For a detailed discussion on the application of these and other accounting policies, see the Company’s Annual Report on Form 10-K for the year ended June 30, 2013.
 
Recently Issued Accounting Guidance
 
See Note 1 – Summary of Significant Accounting and Reporting Policies for more information on recent accounting pronouncements and their impact, if any, on the Company’s financial statements. Management believes there have been no material changes to our critical accounting policies.
 
Item 3.    Quantitative and Qualitative Disclosure about Market Risk
 
At September 30, 2013, the Company did not have any debt outstanding.  The revolving credit facility bears an interest rate using the 30-day LIBOR rate as the basis, as defined in the loan agreement, and therefore is subject to additional expense should there be an increase in market interest rates while borrowing on the revolving credit facility.
 
The Company had no holdings of derivative financial or commodity instruments at September 30, 2013. The Company has international sales; however these sales are denominated in U.S. dollars, mitigating foreign exchange rate fluctuation risk. 
 
Item 4.     Controls and Procedures
 
Evaluation of Disclosure Controls and Procedures
   
The Company maintains controls and procedures designed to ensure that information required to be disclosed in the reports that the Company files or submits under the Securities Exchange Act of 1934 is recorded, processed, summarized, and reported within the time periods specified in the rules and forms of the Securities and Exchange Commission and that such information is accumulated and communicated to the Company's management, including its Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. Based upon their evaluation of those controls and procedures performed as of September 30, 2013, the Chief Executive Officer and Chief Financial Officer of the Company concluded that its disclosure controls and procedures were effective.
   
 
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Changes in internal control over financial reporting
 
There were no changes in the Company’s internal control over financial reporting during the quarter ended September 30, 2013 that have materially affected, or are reasonably likely to materially affect, the registrant’s internal control over financial reporting.
 
Part II.        OTHER INFORMATION
Item 1.  Legal Proceedings          
Dräger Medical GmbH, Draeger Medical Systems, Inc. and Draeger Medical Inc. v. Allied Healthcare Products, Inc., filed in the United States District Court for the District of Delaware, Case No. 1:13-cv-01656-SLR. On or about October 4, 2013, Dräger Medical GmbH and certain affiliates (the “Dräger Plaintiffs”) filed a patent infringement lawsuit against Allied in the District of Delaware, asserting that Allied infringes United States Patent Nos. 7,487,776 and 8,286,633, both protecting particular combinations of carbon dioxide absorption cartridges and adapters which fit on anesthesia machines. The Dräger Plaintiffs assert that Allied’s sales of certain models of its Litholyme and Carbolyme single-use carbon dioxide absorption cartridges infringe both patents.  Allied has answered the Complaint, asserting invalidity of the patents, non-infringement, and implied license under the doctrine of permissive repair.
 
On October 25, 2013, the Dräger Plaintiffs filed a motion for preliminary injunction requesting that Allied be enjoined from selling certain models of its Litholyme and Carbolyme cartridges during the pendency of the litigation. The Court has set a hearing date of January 17, 2014 on the motion for preliminary injunction.
 
The Company cannot estimate a possible loss or range of loss for this matter because damages claimed by the Dräger Plaintiffs have not been specified and the proceedings are in early stages.  The Company intends to vigorously contest the motion for preliminary injunction and defend against the litigation brought by the Dräger Plaintiffs and pursue counterclaims for invalidity, non-infringement, and implied license  
 

Item 6.        Exhibits

 
(a)
Exhibits:
 
31.1  
Certification of Chief Executive Officer (filed herewith)
     
31.2  
Certification of Chief Financial Officer (filed herewith)
     
32.1
Sarbanes-Oxley Certification of Chief Executive Officer (furnished herewith)*
 
 
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32.2
Sarbanes-Oxley Certification of Chief Financial Officer (furnished herewith)* 
   
99.1
Press Release dated November 13, 2013 announcing third quarter earnings*
 
101
Pursuant to Rule 405 of Regulation S-T, the following financial information from the Company’s Quarterly Report on Form 10-Q for the period ended September 30, 2013, is formatted in XBRL interactive data files: (i) Statement of Operations for the three months ended September 30, 2013 and 2012; (ii) Balance Sheet at September 30, 2013 and June 30, 2013; (iii) Statement of Cash Flows for the three months ended September 30, 2013 and 2012; and (iv) Notes to Financial Statements.
 
*Notwithstanding any incorporation of this Quarterly Report on Form 10-Q in any other filing by the Registrant, Exhibits furnished herewith and designated with an asterisk (*) shall not be deemed incorporated by reference to any other filing under the Securities Act of 1933 or the Securities Exchange Act of 1934 unless specifically otherwise set forth therein.
 
 
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SIGNATURE
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
  
 
ALLIED HEALTHCARE PRODUCTS, INC.
 
 
 
/s/ Daniel C. Dunn
 
Daniel C. Dunn
 
  Chief Financial Officer
 
 
 
Date: November 13, 2013
 
 
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