Medical device recalls

Philips recalls Philips — Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechani…

Recall date
June 15, 2021
Source
U.S. Food & Drug Administration (FDA) — recall announcement
Brand / firm
Philips, Philips

Why it was recalled

Potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component in these devices — Defect

What was recalled

Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices

Read the official recall notice →

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