Reported Sep 14, 2022 · Ongoing
Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…
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?
- Philips BiPAP A40, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
- Lot codes and dates
- UDI-DI
1,432 of 1,432 codes
606959042742606959042766606959042797606959067677606959067714606959042834606959067752606959067721606959068025Model No.: 1109596110959811096011111169111117711161531116156CN1111169R1111177Serial No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
- UDI-DI
- Amount recalled
- 1,091 units ***updated Jan 2024*** additional 323 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Stop using this product now
Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.
Using this product could cause serious injury, illness or death — stop using it now.
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