Reported Jul 9, 2025 · Ongoing

BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients…

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. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
Lot codes and dates
  • Part Number 1111178
  • UDI

    2,171 of 2,171 codes

    • 0060959049635
    • Serial No. 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
Amount recalled
5,958 units

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, 7:35 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.