1 Series Phototherapy Device
1 Series Phototherapy Device Recall The 1 Series Phototherapy Device is being recalled in Canada because it does not perform as intended. This recall affects all units of this device that were distributed across Canada. The FDA has classified this as a Class I recall, which is the most serious classification.
- Product
- 1 Series Phototherapy Device
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-06-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a051150c-e45a-494d-aae0-fb60c8f089bf