Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23907 |
| Brand Name: | cobas c311, cobas c702, cobas c501/502 |
| Model: | |
| Affected: | Bilirubin Total Gen.3 cobas c - Tina-quant IgM Gen.2 - Lactate Gen.2 cobas c |
| Software version: | |
| Recalling Organisation: | Roche Diagnostics (NZ) Ltd 15 Rakino Way Mt Wellington AUCKLAND 1644 |
| Contact Information: | 0800 363 622 |
| Manufacturer: | Roche Diagnostics GmbH |
| Issue: | In readiness for the introduction of a new analyser, selected endogenous drug interferences in serum/plasma, urine and CSF (cerebrospinal fluid) were assessed for their potential risk on all Roche tests and corresponding platforms. The cause for the interference is the direct concentration-dependent interaction of the interferent with the test system. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 28/11/2018 |
