Fingertip Pulse Oximeter
Fingertip Pulse Oximeter Recall Fingertip pulse oximeters are being recalled across Canada because they were sold without proper authorization from Health Canada. This is classified as a Class I recall, the most serious type. The devices do not meet required regulatory standards for sale in Canada.
- Product
- Fingertip Pulse Oximeter
- Reason
- Unauthorised device
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-06-27
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ce5eabb8-085c-4d92-800f-cadcad48b2b0