Minimed 630g & 670g Insulin Pump (2019-11-21)
Recall Summary Medtronic is recalling MiniMed 630G and 670G insulin pumps distributed in Canada due to a defect in the devices. The recall affects patients across Canada who use these insulin pump models. The FDA classified this as a Class I recall, indicating a serious safety concern.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-12-06
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b5121135-2548-47a5-b692-52a74a0cde72