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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