Iontoderma Id-1000 (2016-08-08)
IONTODERMA ID-1000 Recall Summary The IONTODERMA ID-1000 medical device has been recalled across Canada. The device was recalled due to issues classified as a Class I concern, which indicates a serious problem with the product. This recall affects all units of this device that were distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-08-10
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1bef45fb-e4bc-44f8-a6a8-96313935e792