Overhead Lift Roomer S And Altair (2016-07-07)
Overhead Lift Roomer S and Altair Recall The Overhead Lift Roomer S and Altair devices are being recalled in Canada due to safety concerns related to their function as medical devices. This recall affects all units distributed across Canada. The FDA has classified this as a Class I recall, indicating a serious safety issue.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-10-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1d7decf0-dbb1-4783-bcd3-77d41f4e0d19