Laris Pump Module Model 8100 (2018-04-10)
Alaris Pump Module Model 8100 Recall The Alaris Pump Module Model 8100 infusion pump is being recalled across Canada due to a safety concern with the medical device. This recall affects healthcare facilities and settings where this pump model is used to deliver medications to patients. The FDA classified this as a Class I recall, indicating the most serious type of safety issue.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-05-04
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fc1476ce-9b83-4401-83cf-959b198a16bc