Vitek 2 Gp Id (2017-10-16)
VITEK 2 GP ID Recall Summary The VITEK 2 GP ID system, a medical device used to identify bacteria, is being recalled in Canada due to safety or effectiveness concerns. This recall affects units distributed across Canada and has been classified as a Class I recall, which indicates a serious issue. The recall applies to this specific identification system used in medical laboratories.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-10-30
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1215ae55-546a-48a0-970d-5beda05103b5