Cobas 6800, 8800 (2019-06-13)
COBAS 6800, 8800 Recall Summary Roche Diagnostics is recalling COBAS 6800 and 8800 laboratory instruments across Canada due to a medical device issue classified as Class I, which indicates a serious potential health risk. These automated diagnostic systems are used in hospitals and laboratories to process patient samples. The recall affects all units of these devices that were distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-07-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d518ca4b-b8fe-405b-b4b8-758647ea9793