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[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

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductVITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic
Brand / manufacturerOrtho-Clinical Diagnostics
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0914-2018
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date22 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.

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