ProductGuru
AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

[Recalled] T-Cell Xtend REF TTK.610 US — Due to equipment failure, affected products were stored at temperatures outside… | FDA 2022-07-07

recall fda device united-kingdom

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

Recall details

ProductT-Cell Xtend REF TTK.610 US
Brand / manufacturerOXFORD IMMUNOTEC LTD
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1642-2022
Country of noticeUnited Kingdom
Risk levelClass II
Hazard typerecall
Notice date07 July 2022
EAN / barcode15051716000022

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated storage time.

This Class II recall concerns device products distributed in United Kingdom 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 OXFORD IMMUNOTEC LTD

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.

Shop Recalled Cell Xtend REF
Search on Amazon ›Find on eBay ›
As an Amazon Associate and eBay Partner, we may earn from qualifying purchases.
Related articles

Explore by topic

Looking up a product? Use ProductGuru — free barcode & product database with 35M+ products. Search by EAN / UPC barcode.
Was this page helpful?