Zymutest Hia Monostrip Igg & Iggam(2019-07-23)
Recall Summary ZYMUTEST HIA MonoStrip IgG & IgGAM medical devices are being recalled in Canada due to a safety or effectiveness issue. This is a Class I recall, which is the most serious type. The affected devices were distributed across Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-08-09
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/10e9e6dc-c67d-40c4-8b86-14a19d00db39