Microtek Decanter Devices
Microtek Decanter Devices are being recalled across Canada because they are unapproved medical devices that do not meet sterility requirements. These devices were distributed without authorization. This is a Class I recall, which is the most serious classification.
- Product
- Microtek Decanter Devices
- Reason
- Sterility - Unauthorised device
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-06-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/679a3c0b-54b7-4ef3-ae6a-8b6f883478ad