17 Alpha-hydroxyprogesterone Elisa Kit (2018-05-04)
Recall Summary A 17 Alpha-HydroxyProgesterone ELISA Kit used for laboratory testing has been recalled across Canada. The kit is a Class I medical device recall, meaning there is a potential serious adverse health consequence or death. The recall affects all locations in Canada that received this product.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-06-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a415bec3-0048-4292-9be0-3a927c2fca54