[Recalled] VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic — This product is not meeting the current storage labeling for unopened VITROS DA… | FDA 2017-09-22
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic |
|---|---|
| Brand / manufacturer | Ortho-Clinical Diagnostics |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0914-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 22 September 2017 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: This product is not meeting the current storage labeling for unopened VITROS DAT Performance Verifiers causing customers to obtain lower than expected VITROS BENZ results when using this control.
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 Ortho-Clinical Diagnostics
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.