Laris Pca And Syringe Module Models (2017-11-23)
Alaris PCA and Syringe Module Recall Baxter is recalling certain Alaris PCA (patient-controlled analgesia) and Syringe Module models distributed across Canada due to a safety issue with the medical devices. The recall affects infusion pump modules used to deliver medication to patients. This is classified as a Class I recall, meaning there is a serious potential for adverse health consequences.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-12-08
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/86bff419-5918-4801-bb93-5d49ae487192