Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2036-2025 — 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.

U.S. FDA — Device Enforcement · United States · 2025-05-09 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2036-2025
Date of alert
2025-05-09
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Philips Respironics, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00606959021532
Reported risk: This device does not indicate for use in patients with respiratory failure.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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