Reported May 29, 2024 · Ongoing

BiPAP V30 Auto Ventilator, Part Number 1111178

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 V30 Auto Ventilator
    • Part Number 1111178
Lot codes and dates
  • UDI-DI 00606959049635 Serial Numbers

    2,326 of 2,326 codes

    • N2068642229E4
    • N206864244CD2
    • N206864255D5B
    • N206864277E49
    • N2068642886BE
    • N206864299737
    • N2068643102A7
    • N20686432303C
    • N2068643321B5
    • N20686434550A
    • N206864354483
    • N206864367618
    • N206864376791
    • N206864389F66
    • N206864398EEF
    • N206864405E26
    • N206864414FAF
    • N206864427D34
    • N206864441802
    • N20686445098B
    • N206864463B10
    • N206864472A99
    • N20686448D26E
    • N20686449C3E7
    • N2068645047FE
    • N206864515677
    • N2068645264EC
    • N206864537565
    • N2068645401DA
    • N206864551053
    • N2068645622C8
    • N206864573341
    • N20686458CBB6
    • N206864606D96
    • N206864617C1F
    • N206864624E84
    • N206864635F0D
    • N206864653A3B
    • N2068646608A0
    • N2070799636A7
    • N20708029041F
    • N20708103C229
    • N20708105A71F
    • N2070811974AB
    • N20708120C302
    • N20708137AE65
    • N20708141865B
    • N20708147E36D
    • N20713207A038
    • N20713212EE4D
    • N207132184117
    • N20713222C425
    • N20713232DDFD
    • N2071323872A7
    • N20713245E44A
    • N207132582677
    • N20713270998F
    • N207132810BCE
    • N2071329445BB
    • N2071329666A9
Amount recalled
5,958 US; None OUS

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Stop using this product now

Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.

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, 5:42 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.