Bd Alaris
BD Alaris Recall Summary BD Alaris infusion pumps are being recalled across Canada because they are unauthorized medical devices. This is a Class I recall, which is the most serious classification. The recall affects BD Alaris products distributed throughout Canada.
- Product
- Bd Alaris
- Reason
- Unauthorised device
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-02-28
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d8446b97-5ded-4833-b47a-c40f43c886d1