Reported Sep 14, 2022 · Ongoing
Philips BiPAP A30, 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 A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
- Lot codes and dates
- UDI-DI
204 of 204 codes
606959042667606959042681606959042698606959042728606959067585606959067530Model No.: 110958111095821109585110958811095891109590110959411095961109598110960111111241111150111115511111691111177111117811161531116156CN1111143CN1111169R1111124R1111177Serial No.: N287725308B25N28870219ADAEN288702267F31N2887023003DFN288702473A68N28870248C29FN2887025723B0N28870279F97EN28870300736BN2887030162E2N2887030341F0N288703153D1EN288703341F27N28870339C4C2N288703423719N2887034989CAN288703533F48N288710382694N28871040E7D4N28871042C4C6N28871043D54FN28871045B079N28871047936BN288710486B9CN28872243453AN28872424B38CN28872434AA54N30471136FB91N304711485FE7N30471153F8ECN30471195347AN30471199FE16
- UDI-DI
- Amount recalled
- 146 units ***updated January 2024*** 30 additional 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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