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Recall Observatory FDA recall evidence

Device product

BiPAP A30, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111143

Z-1629-2021

April 06, 2021

Class II

Product summary

Firm
Philips Respironics, Inc.
Event
Event 87753
Status
Terminated
Classification
Class II
Quantity
2 units
Official record key
device-enforcement:Z-1629-2021

Official wording

Reason: Certain devices were built with motor assemblies that could contain non-conforming plastic material. This could result in 1. Exposure to off-gassing of Volatile Organic Compounds not normally present creating a potential biosafety or toxicological hazard and 2. Sudden failure of the device causing a Ventilator Inoperative condition with the potential for asphyxia if not immediately identified and addressed by the care provider.

Code information: Serial Number: N306151248079, N306164395E34

Distribution pattern: Distribution US nationwide to states of: LA, PA, WI, CO, WV, WA, CA, TX, MO, OK, FL, and TN. Brazil, China, and Japan

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Certain devices were built with motor assemblies that could contain non-conforming plastic material. This could result in 1. Exposure to off-gassing of Volatile Organic Compounds not normally present creating a potential biosafety or toxicological hazard and 2. Sudden failure of the device causing a Ventilator Inoperative condition with the potential for asphyxia if not immediately identified and addressed by the care provider.