[Recalled] Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component. — Units from one batch of TriFit TS size 2 stem were found to be labeled as a Tri… | FDA 2021-05-06
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Corin TriIFit TS SIZE 2, STANDARD TAPERED STEM, CEMENTLESS, REF 694.0002. Hip prosthesis component. |
|---|---|
| Brand / manufacturer | Corin Ltd |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1850-2021 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 May 2021 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.
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 Corin 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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