[Recalled] RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome. — DNAs used during the manufacture of two affected models were accide
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome. |
|---|---|
| Brand / manufacturer | Cytocell Ltd. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2210-2023 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 May 2023 |
| EAN / barcode | 05055844900516 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: DNAs used during the manufacture of two affected models were accidentally inverted during manufacturing.
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 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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