Cobas 6500 Cobas U 601 And U 701 (2018-06-20)
Summary Roche is recalling Cobas 6500, Cobas u 601, and Cobas u 701 laboratory analyzers across Canada due to a defect in the medical device. The recall is classified as Class I, meaning the devices could cause serious harm or death. These analyzers are used in hospital and clinical laboratories to process patient test samples.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-07-27
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fbbe0ab2-40c5-4560-9a14-09d7a143fee3