[Recalled] cobas HCYS, Homocysteine Enzymatic Assay, Material Number REF 06542921190, for use on cobas c 701/702, in vitro test for total L-homocysteine — Abnormal calibration signals and control recovery issues on the Homocysteine En… | FD
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | cobas HCYS, Homocysteine Enzymatic Assay, Material Number REF 06542921190, for use on cobas c 701/702, in vitro test for total L-homocysteine |
|---|---|
| Brand / manufacturer | Roche Diagnostics Operations, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0489-2025 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 17 October 2024 |
| EAN / barcode | 04015630929979 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Abnormal calibration signals and control recovery issues on the Homocysteine Enzymatic (HCYS) Assay can produce erroneous patient results (positive or negative bias)
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Roche Diagnostics Operations, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.