Laris Pump Module Model 8100 (2017-06-12)
Alaris Pump Module Model 8100 Recall Summary The Alaris Pump Module Model 8100 is being recalled across Canada due to a safety issue with the medical device. This recall affects healthcare facilities and patients who use this infusion pump model. The FDA classified this as a Class I recall, indicating a serious potential health risk.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-09-26
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/937c1f88-f2c6-4f1a-9a23-0e4441878678