Ambu® Spur®ii Adult And Pediatric Resuscitator
Ambu® SPUR®II Adult and Pediatric Resuscitator Recall Ambu® SPUR®II Adult and Pediatric Resuscitator devices are being recalled across Canada due to a performance issue. The devices are manual resuscitators used to deliver oxygen and assist breathing in patients. This is a Class I recall, which means the product could cause serious harm or death.
- Product
- Ambu® SPUR®II Adult and Pediatric Resuscitator
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-07-23
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9d9a65ad-e417-4f44-aa8e-9dd5efc92ca5