[Recalled] Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent. — There is an error in the chromomap included in the labeling for the product | FDA 2019-03-15
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Aquarius CSF1R/RPS14 (5q32-q33) Probe Red, Model LPH540-A Analyte specific reagent. |
|---|---|
| Brand / manufacturer | Cytocell Ltd. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1202-2019 |
| Country of notice | United Kingdom |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 15 March 2019 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: There is an error in the chromomap included in the labeling for the product.
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 →
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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.