RecallRadar

FDA Device recall Z-1626-2021

BiPAP A40, China: Continuous ventilator, non-life-supporting

On 2021-06-02 the FDA classified a Class II recall of BiPAP A40, China: Continuous ventilator, non-life-supporting by Philips Respironics, citing 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….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1626-2021
ClassificationClass II
Statusterminated
Initiated2021-04-06
Published2021-06-02
Last updated2026-09-13 11:56 UTC
CompanyPhilips Respironics
DistributionUS

Product

BiPAP A40, China: Continuous ventilator, non-life-supporting. Material Number - CN1111169

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.

Identifiers

code_info
Serial Number: V30446637ACAE, V30446653BE5A, V304441360854, V304457587F98, V304468408502, V304441766F34, V3044555732D7,…Serial Number: V30446637ACAE, V30446653BE5A, V304441360854, V304457587F98, V304468408502, V304441766F34, V3044555732D7, V30446846E034, V30444034719A, V3044642346EA.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1626-2021%22

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