Bioplex 2200 Ebv Igm Control Set (2018-11-21)
BioPlex 2200 EBV IgM Control Set Recall The BioPlex 2200 EBV IgM Control Set, used in laboratory testing for Epstein-Barr virus antibodies, has been recalled across Canada. The recall was issued due to issues with the medical device itself. This affects laboratories and healthcare facilities that use this control set for diagnostic testing.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-12-10
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/c6bf1801-f9d3-4503-ba01-1d75b7e0deff