Bioplex 2200 Ana Screen Control Set (2019-02-05)
BioPlex 2200 ANA Screen Control Set Recall The BioPlex 2200 ANA Screen Control Set, a medical device used in laboratory testing, is being recalled across Canada. The recall was classified as Class I, meaning there is a serious potential health risk. The product was distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-03-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/eab5cb7f-327c-4d63-9333-5f851642b405