Bd Alaris™ Pump Module
BD Alaris™ Pump Module Recall Summary BD is recalling the Alaris™ Pump Module across Canada due to a performance issue. The recall is classified as Class I, meaning there is a serious potential health risk. This recall affects the Alaris™ Pump Module product, which is a drug delivery device used in healthcare settings.
- Product
- BD Alaris™ Pump Module
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-10-29
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/6c3a2e78-7fd0-4db3-bd37-d27a9698ea7d