Reported Jul 9, 2025 · Ongoing
BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing…
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 A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric patients weighing more than 10 kg. BiPAP Hybrid A30 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients.
- Lot codes and dates
BiPAP A30 Part No. 11111431111144CN1111143111114511111471111149111114811111501116155BR11111431111144M1111144L1111144VR10764911111154R111114311011091109594107654010765811076583107658211111451076581
- UDI
2,155 of 2,155 codes
0060695902153200606959039308006069590393150060695903933900606959039346006069590393530060695903936000606959039384006069590393910060695904272800606959048744006069590487510060695904876800606959067530006069590676600060695941267500606959412699Serial No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
- Amount recalled
- 3 units in US 22,416 units and 49 units OUS
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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