Reported Jul 9, 2025 · Ongoing

BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric…

Philips Respironics, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips Respironics, Inc. · 1001 Murry Ridge Ln · Murrysville, PA · 15668-8517

Is this the product you have?

  • BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
Lot codes and dates
  • USA40 Material No. 1111169 UDI-DI 00606959039476 Serial Numbers V182393118CC9 V21942863DD70 V219429359C22 V25585948745C
  • V26439189762A V2640770372E7 OUSA40: Material No. 1111169 UDI-DI 00606959039476 Serial Numbers

    2,313 of 2,313 codes

    • V09765327781A
    • V09765332366F
    • V097653405875
    • V097653436AEE
    • V097653472CCA
    • V0976535041AD
    • V097653551600
    • V09765356249B
    • V09765358CDE5
    • V100863961519
    • V10086398FC67
    • V10086399EDEE
    • V100864020820
    • V10086408A77A
    • V1008641032EA
    • V100864112363
    • V100864130071
    • V1008641474CE
    • V100864201882
    • V100864223B90
    • V100864276C3D
    • V10086436646C
    • V100864388D12
    • V100864399C9B
    • V100864426F40
    • V100864437EC9
    • V100864462964
    • V10086448C01A
    • V10086450558A
    • V100864514403
    • V100864527698
    • V100864536711
    • V100864550227
    • V1008645630BC
    • V10086459C84B
    • V100864616E6B
    • V100864634D79
    • V1008646439C6
    • V10086465284F
    • V100864670B5D
    • V10086468F3AA
    • V1008643333C1
    • V1008647177B3
    • V100864724528
    • V100864771285
    • V10086478EA72
    • V10086479FBFB
    • V1008648869BA
    • V100864013ABB
    • V100864267DB4
    • V100864451BFF
    • V10086458D9C2
    • V100864625CF0
    • V100864753197
    • V10086484A3D6
    • V10086476030C
    • V10086509EC2F
    • V100865489AC6
    • V10086482C6E0
    • V1008643556F7
Amount recalled
6 units in US 67534 OUS

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Stop using this product now

This device does not indicate for use in patients with respiratory failure.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:59 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.