Vidas Lyme Igg II (2016-03-14)
VIDAS Lyme IGG II Recall Summary The VIDAS Lyme IGG II medical device, used for detecting Lyme disease antibodies, was recalled across Canada in March 2016 due to a Class I safety issue. This classification indicates a serious problem with the device that could affect patient health or safety. The recall affected the device throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-04-04
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9ea163ff-7767-47b4-af45-445c4eaed070