Health product recall

Philips BIPAP A40 Pro ventilators

Last updated

Summary

Product
Philips BIPAP A40 Pro ventilators
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

BiPAP A40 Pro, Ca W/ Heated Tube Humidifier, Ca

All lots.

CAX3100T12

BiPAP A40 Pro, Ca

All lots.

CAX3100S12

Issue

Philips Respironics has become aware of a potential safety issue with all BIPAP A40 Pro ventilators.  The ventilator may incorrectly generate a "high internal oxygen" alarm.  To date, there have been no instances of patient harm or injury reported to Philip Respironics caused by this potential issue.

Recall start date: July 16, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Anaesthesiology
Companies

Respironics Inc. Also Trading As Philips Rs North America LLC

1001 Murry Ridge Lane, Murrysville, Pennsylvania, United States, 15668

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75857

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