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[Recalled] Vancomycin Screen Agar — The affected expired lots of product may have exhibited breakthrough growth of… | FDA 2015-06-29

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

ProductVancomycin Screen Agar
Brand / manufacturerBecton Dickinson & Co.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0473-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date29 June 2015

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The affected expired lots of product may have exhibited breakthrough growth of vancomycin susceptible Enterococcus facaelis ATCC 29212 near the end of shelf life. The in-date product may also exhibit breakthrough growth of vancomycin susceptible Enterococcus facaelis ATCC 29212 near the end of shelf life.

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 Becton Dickinson & Co.

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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