[Recalled] 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 o
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | 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. |
|---|---|
| Brand / manufacturer | Philips Respironics, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2036-2025 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 09 May 2025 |
| EAN / barcode | 00606959021532 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: This device does not indicate for use in patients with respiratory failure.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.