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[Recalled] TCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome Catalog Number: LPH046-A — May show unexpected locus specific signals in addition to thos

recall fda device united-kingdom

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductTCL1 Breakapart Probe, Fluorescence in situ hybridisation (FISH) is a technique allows the visualisation of DNA sequences upon chromosome Catalog Number: LPH046-A
Brand / manufacturerCytocell Ltd.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0814-2022
Country of noticeUnited Kingdom
Risk levelClass III
Hazard typerecall
Notice date04 February 2022

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: May show unexpected locus specific signals in addition to those at 14q32.

This Class III 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 Cytocell 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.

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