Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21213 |
| Brand Name: | Roche Cobas c |
| Model: | |
| Affected: | Cobas c311: Catalogue No. 05899427001, cobas c501, c502: Catalogue No. 04547241001, cobas c702, cobas 8000 ISE: Catalogue No. 04945794001 |
| Software version: | |
| Recalling Organisation: | Roche Products (NZ) Ltd 98 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | |
| Manufacturer: | Roche Diagnostics GmbH |
| Issue: | In very rare cases where the disturbance of the sample liquid level detection (LLD) occurs, the affected sample probe may dip into the sample material deeper than intended, the affected sample probe may be not washed adequately. This may lead to carryover. |
| Recall action type: | Recall |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 14/3/2017 |
