Ivea Model 500a (2017-10-11)
IVEA Model 500A Recall Summary The IVEA Model 500A medical device is being recalled across Canada due to a Class I safety issue. This is the most serious type of recall, indicating the device could cause serious injury or death. The recall affects all units of this model distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-10-27
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/c74970bb-0461-46de-8997-42923f6a6fc0