ALLIED HEALTHCARE PRODUCTS INC
8-K, 1999-02-04
ORTHOPEDIC, PROSTHETIC & SURGICAL APPLIANCES & SUPPLIES
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                       SECURITIES AND EXCHANGE COMMISSION
                              WASHINGTON, DC  20549


                                    FORM 8-K

                                 CURRENT REPORT
                     PURSUANT TO SECTION 13 OR 15(d) OF THE
                         SECURITIES  EXCHANGE ACT OF 1934


                        Date of report:  February 4, 1999


                        ALLIED HEALTHCARE PRODUCTS, INC.
               (Exact Name of Registrant as Specified in Charter)


             Delaware               0-19266                      23-1370721
(State  or  Other  Jurisdiction   (Commission                 (IRS  Employer
         of  Incorporation)       File  Number)             Identification  No.)


       1720  Sublette  Avenue
        St.  Louis,  Missouri                                      63110
(Address  of  Principal  Executive  Offices)                    (Zip  Code)

                                 (314) 771-2400
              (Registrant's telephone number, including area code)




                                   Page 1 of 8
<PAGE>

ITEM  5.     OTHER  EVENTS.

     On  February  4,  1999, the Registrant issued a news release announcing its
recall of all oxygen regulators sold under the Life Support Products (LSP) brand
to  replace  aluminum components in the units' high-pressure chambers with brass
components.  The  Registrant  news  release issued on February 3, 1999, attached
as Exhibit 1 hereto, is incorporated herein by reference and made a part hereof.
In  addition,  attached hereto as Exhibit 2 and incorporated herein by reference
and  made  a part hereof is a proposed advertisement that the Registrant intends
to  place  in  certain  national  publications  relating  to  such  recall.




                                   Page 2 of 8
<PAGE>

                                   SIGNATURES

     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  hereunto  duly  authorized.

                              ALLIED  HEALTHCARE  PRODUCTS,  INC.


Date:  February  4,  1999            By:    /s/    Uma  Nandan  Aggarwal
                                            ----------------------------
                                            Name:  Uma  Nandan  Aggarwal
                                            Title:     Chief  Executive  Officer




                                   Page 3 of 8
<PAGE>

                                  EXHIBIT INDEX


Exhibit  No.          Description                                   Page  No.
- ------------          ----------------------------------------      ---------

1.                    News  Release  dated  February  5,  1999              5

2.                    Proposed  Advertisement                               7


                                   Page 4 of 8
<PAGE>

Exhibit  1  -  Press  Release

FOR  IMMEDIATE  RELEASE

Contact:  Tom  Goyda  or  Beth  Randolph
          Shandwick  International
          (314)  436-6565

                       ALLIED HEALTHCARE PRODUCTS ANNOUNCE
                         RECALL OF LSP OXYGEN REGULATORS

         COMPANY TO TAKE SECOND QUARTER CHARGE TO COVER ASSOCIATE COSTS

ST.  LOUIS,  February  4  1999-Allied Healthcare Products, Inc. (NASDAQ:AHPI) is
recalling all oxygen regulators sold under the Life Support Products (LSP) brand
to  replace  aluminum components in the units' high-pressure chambers with brass
components.  The  action  is  being  taken  in  response to reports of fires and
explosions,  the  exact  causes  of  which  remain  unknown.

     The models subject to this recall consist of the LSP 106, LSP 270, LSP 280,
LSP 370, and LSP 735 series regulators.  LSP Oxygen regulator users will be able
to  have  the  parts  replaced  at  pre-existing  authorized  service  centers
nationwide.

     This  recall is being undertaken in cooperation with the United States Food
and  Drug  Administration to minimize the potential for fires and explosions, an
inherent  risk  with  any  high-pressure  oxygen  delivery  system.  Fires  and
explosions  can  occur  in the tanks, post valves and regulators of such systems
when virtually any type of contaminants - including hydrocarbons, metal shavings
or  even  dust  particles  -  are  present  or  introduced  during  handling and
maintenance,  or  when  the  tanks  are  refilled  with  gas.

     In  May, 1997, Allied conducted a recall to add a bronze sintered filter to
the  LSP 270 Series regulator only.  All of the LSP 270 Series regulators should
already  be  fitted  with a sintered bronze filter.  ALTHOUGH THE LSP 270 SERIES
REGULATOR  MAY HAVE ALREADY BEEN RETROFITTED WITH THE SINTERED BRONZE FILTER, IT
IS  ESSENTIAL  THAT  THE  INTERNAL  HIGH-PRESSURE  PARTS  BE REPLACED WITH BRASS
COMPONENTS  TO  ENHANCE  SAFETY.  All  LSP  regulators without a bronze sintered
filter  and  all  regulators  manufactured  by  LSP's  predecessor  corporation,
Robertshaw  Controls  Company, Inc., should be taken out of service IMMEDIATELY.
If  the  user  is  unable  to  determine  if  a  sintered bronze filter has been
installed,  Allied  should  be  contacted  for assistance in this determination.

     Due  to  industry-wide  fires  and  Allied's  understanding that the FDA is
recommending  the  elimination  of all aluminum in oxygen regulators, Allied has
voluntarily  initiated  the recall to replace all high-pressure parts with brass
parts.  THIS  IS STRICTLY AN INTERIM MEASURE which will enable the regulators to
be  used  during  the  period  required to manufacture the new brass regulators.
Allied  will  issue  another  notification  when the new brass regulators become
available.

                                   Page 5 of 8
<PAGE>

     "This  recall  reflects  Allied's  strong  commitment  to manufacturing the
highest  quality  products  and to the safety of all of our customers," said Uma
Nandan  Aggarwal,  Allied's  Chief  Executive  Officer.

     Allied  is  aggressively undertaking development and enhancement of its new
brass regulators series and will be making available a trade-in program once the
new  brass  regulators  are  available.

     Users  can reduce risk during use of any oxygen regulators, keeping in mind
the  following  precautions:

     >     The  oxygen  tank,  post  valve  and  regulator should be free of all
contaminants;

     >     The  post  valve  should  be open slowly whenever the unit is used to
minimize  heat  of  rapid  compression  in  the  regulator.

     >     Users who refill their own oxygen cylinders should take extra care to
avoid  the  introductions  of  containments  during  the  filling  process.

     Allied  will  have  its  authorized  service centers equipped to handle the
recall  within  the next few weeks.  Customers should receive a mailing with the
details  about  how  to  have  their  regulators  serviced.

     Allied  also announced that the company expects to take a one-time, pre-tax
charge of approximately $1.5 million, or 12 cents per share after tax, for costs
associated  with  the recall.  The charge will be recorded in the second quarter
of  Allied's  fiscal  1999,  which  ended  December  31,  1998.


                                   Page 6 of 8
<PAGE>


Exhibit  2  -  Form  of  Advertisement

HED:      ATTENTION  FIRE  AND  EMERGENCY  SERVICES  PERSONNEL

SUBHED:   Recall  of  Life  Support  Products  (LSP)  Oxygen  Regulators

BODY:     Allied  Healthcare  Products,  Inc. is recalling all oxygen regulators
          sold under the Life Support  Products (LSP) brand to replace  aluminum
          components in the units' high-pressure chambers with brass components.
          This  action  is being  taken in  response  to  reports  of fires  and
          explosions, the exact causes of which remain unknown.

               LSP oxygen  regulators  users will be able to have the  regulator
               parts on their  LSP 106,  LSP 270,  LSP 280,  LSP 370 and LSP 735
               series   regulators   replaced  at  authorized   service  centers
               nationwide.

               This recall is being  undertaken in  cooperation  with the United
               States  Food  and  Drug  Administration  (FDA)  to  minimize  the
               potential  for fires and  explosions,  an inherent  risk with any
               high-pressure oxygen delivery system.

               In May 1997,  Allied  conducted a recall to add a sintered bronze
               filter to the regulator.  All regulators should already be fitted
               with  this  sintered  bronze  filter.  ANY  REGULATORS  WITHOUT A
               SINTERED  BRONZE FILTER AND ALL REGULATORS  MANUFACTURED BY LSP'S
               PREDECESSOR  CORPORATION,   ROBERTSHAW  CONTROLS  COMPANY,  INC.,
               SHOULD BE TAKEN OUT OF SERVICE IMMEDIATELY.  If the regulator was
               bought  after May 1997 or  retrofitted  pursuant  to the May 1997
               recall,  the regulator  should  already have the sintered  bronze
               filter installed.

               This, in conjunction with present recall efforts,  will result in
               the  replacement of all aluminum  high-pressure  parts with brass
               parts. This interim measure will enable the regulators to be used
               during   the  period   required   to   manufacture   non-aluminum
               regulators.  This information has been provided to the FDA. It is
               Allied's   understanding   that  the  FDA  is  recommending   the
               elimination of all aluminum in oxygen regulators.

               Allied  will be making  available  a trade-in  program on its new
               brass regulators once this transition is complete.

               Users can  reduce  risk  during use of any  oxygen  regulator  by
               keeping in mind the following precautions:

                    The oxygen tank, cylinder valve and regulator should be free
                    of all contaminants.

                                   Page 7 of 8
<PAGE>

                    The cylinder valve should be opened slowly whenever the unit
                    is  used  to  minimize  heat  of  rapid  compression  in the
                    regulator.

                    Users who refill  their own  oxygen  cylinders  should  take
                    extra care to avoid the introductions of contaminants during
                    the filling process.

               Allied  will have its  authorized  service  centers  equipped  to
               handle the recall  within  the next few weeks.  Customers  should
               receive  a  mailing  with the  details  about  how to have  their
               regulators serviced.  Additional  information  concerning the new
               brass regulators will shortly be forthcoming.

Contact:     Recall  Coordinator

Telephone:   (800)  216-4624  (Monday through Friday between the hours  of  8:00
             a.m.  and  5:00  p.m.  CST)

Fax:         (888)  231-5273

Mail:        LSP  Regulator  Recall  Center
             Allied  Healthcare  Products,  Inc.
             1720  Sublette  Blvd.
             St.  Louis,  MO  63110

E-mail:      [email protected]


                                   Page 8 of 8
<PAGE>


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