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[Recalled] Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency. — Motor assemblies manufactured with nonconforming plastic that contr

recall fda device united-states

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductPhilips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea syndrome (OSA) and respiratory insufficiency.
Brand / manufacturerPhilips Respironics, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1654-2022
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date26 August 2022
EAN / barcode606959042667

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Motor assemblies manufactured with nonconforming plastic that contributes to off-gassing of VOCs.

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 →

Related recalls from Philips Respironics, Inc.

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.

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