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Philips bipap a40 pro ventilators
Official notice
24 Jul 2024
Last checked
24 Jul 2024
An official Health Canada notice concerns Philips bipap a40 pro ventilators. 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 Published 2024-07-24.
What to do now
Contact the manufacturer if you require additional information.
Recall number
75857
Official notice
2024-07-24
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Product 2
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Philips.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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