Device recall
Z-2070-2013: TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0143/18, Stem size 03…
FDA device recall · Class II · Waldemar Link GmbH & Co. KG (Corp. Hq.)
Key facts
| Recall number (Z-number) | Z-2070-2013 |
|---|---|
| Recall event | 65800 |
| Product | TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0143/18, Stem size 03, prox. Stem dia. 18 mm, Length 250 mm, WALDEMAR LINK GmbH & CoKG, Barkhausenweg 10 . D . 22339 Hamburg |
| Product code | HWT |
| Recalling firm | Waldemar Link GmbH & Co. KG (Corp. Hq.) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2014 |
| 510(k) numbers | K955296 |
| FEI number | 3002808472 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database