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Allied Healthcare Products, Inc.

United StatesFDA applicant, unverified

Devices
26
FDA recalls
9

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Allied Healthcare Products, Inc. makes

Allied Healthcare Products, Inc. manufactures respiratory support devices, including portable and emergency ventilators such as the AHP 300, BabyBird, and MCV100 mass casualty ventilator, along with battery packs for emergency use. The company also produces monitoring tools like blood pressure devices and a resuscitation timer (Model L770-CPR), as well as spirometry systems (L.A.P. II). Additional offerings include suction pump cabinets, a mass spectrometer (Medspect II), and mist nebulizers (Schuco Mist and Schuco Deluxe Mist).

The company’s products are regulated under FDA’s 510(k) pathway and fall into Class I and Class II device classifications. These devices are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. Allied Healthcare Products, Inc. is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue26

Newest first, rows 1-26 of 26

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Rows 1-26 of 26

FDA recalls9

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

  • 2010

    • 12 Aug 2010 Z-2152-2011 Unclassified (pre-2012) Terminated The granules do not absorb as long as expected in the anesthesia machines Distribution: Worldwide Distribution - USA including AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MD, MS, NC, NE, NY, OH, OR,…
      Full distribution text Worldwide Distribution - USA including AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MD, MS, NC, NE, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, and WI and the countries of Canada and Grenada.

  • 2009

    • 15 May 2009 Z-2031-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2032-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2033-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2034-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2035-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2036-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2037-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
    • 15 May 2009 Z-2038-2009 Unclassified (pre-2012) Terminated Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position. Distribution: Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.

Frequently asked questions

How many devices does Allied Healthcare Products, Inc. have in the registry?

The registry currently lists 26 devices for Allied Healthcare Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Allied Healthcare Products, Inc.'s devices?

Among its 26 most recently registered devices, Allied Healthcare Products, Inc. has devices listed in FDA 510(k) (26 devices).

What risk classes do Allied Healthcare Products, Inc.'s devices fall under?

Among its 26 most recently registered devices, the classes recorded for Allied Healthcare Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Allied Healthcare Products, Inc.?

FDA recall records list 9 recalls initiated by Allied Healthcare Products, Inc., the most recent initiated on 12 Aug 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Allied Healthcare Products, Inc. in the registry?

The most recently registered devices listed for Allied Healthcare Products, Inc. include SCHUCO MIST AND SCHUCO DELUXE MIST, MASS SPECTROMETER-MEDSPECT II, GOMCO SUCTION PUMP CABINET CHANGE and BEAR CUB INFANT PRESSURE VENTILATOR.

Generated automatically from registry data and not verified by a human reviewer.