Laris Pump Module, Model 8100 (2019-04-12)
Recall Summary Alaris Pump Module Model 8100 devices have been recalled across Canada due to a medical device issue. This recall affects all units of this infusion pump model that were distributed in Canada. The FDA has classified this as a Class I recall, indicating a serious potential health risk associated with the device.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-05-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/08b3611a-16f6-415f-a4c2-364c96d5a8fe