Primus Anaesthetic Workstation
Primus Anaesthetic Workstation Recall The Primus Anaesthetic Workstation is being recalled due to a manufacturing defect. This device is used in hospitals and medical facilities across Canada to deliver anesthesia to patients during procedures. The FDA has classified this as a Class I recall, which indicates a serious issue with the equipment.
- Product
- Primus Anaesthetic Workstation
- Reason
- Manufacturing defect
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-05-10
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2f33a9c7-0fa6-4e52-bca7-37f8364dfc46