Her2 Cish Pharmdx Kit (2016-06-10)
HER2 CISH PharmDX Kit Recall Summary The HER2 CISH PharmDX Kit, a medical device used for diagnostic testing, was recalled in Canada on June 10, 2016. The recall was classified as Class I, meaning the product could cause serious harm or death. The kit was distributed across Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-07-07
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/85dec317-7114-4e88-ac50-d51e78ee7455