[Recalled] TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0142/20, Stem size 004, prox. Stem dia. 20 mm, Length 210 mm, WALDEMAR LINK GmbH & CoKG, Barkhausenweg 10 . D . 22339 Hamburg — The trial stems were manufactured using the wro
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0142/20, Stem size 004, prox. Stem dia. 20 mm, Length 210 mm, WALDEMAR LINK GmbH & CoKG, Barkhausenweg 10 . D . 22339 Hamburg |
|---|---|
| Brand / manufacturer | Waldemar Link GmbH & Co. KG (Corp. Hq.) |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2064-2013 |
| Country of notice | Germany |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 16 July 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The trial stems were manufactured using the wrong design.
This Class II recall concerns device products distributed in Germany 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.