Reported Jul 21, 2021 · Ongoing
A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting
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?
A-Series BiPAP A 40A-Series BiPAP A30 Continuous VentilatorNon-life Supporting
- Lot codes and dates
- All Devices manufactured before 26 April 2021, All device serial numbers. Material Numbers
83 of 83 codes
107649210764931076495107653810765391076565107656610765791076580107658310765841076586107822610782971104171111116811111691111170111117111111721111173111117411111751111176111117711161561122129114079811407991111170S1111170-SAR1111169BR1076493BR1076566BR1111169CN1076493CN1076566CN1111169GB-SPK0011GB-SPK0012IT1111169LA1076493LA1076566R1076495R1111169R1111177R11161561104170R1111175RBR1111169U1116156103891610389171040716104411410442351038987104071710689421068943
- All Devices manufactured before 26 April 2021, All device serial numbers. Material Numbers
- Amount recalled
- 72665
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
- Nationwide
Why it was recalled
Stop using this product now
The polyester-based polyurethane (PE-PUR) foam may degrade into particles which may enter the devices air pathway and be ingested or inhaled by the user, and the PE-PUR foam may off-gas certain chemicals.
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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