Device recall
Z-2541-2011: Bio-modular reverse shoulder humeral tray with lock ring, 44 mm 10 degree angle…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-2541-2011 |
|---|---|
| Recall event | 58571 |
| Product | Bio-modular reverse shoulder humeral tray with lock ring, 44 mm 10 degree angle, sterile, single use, REF 11-113685, Biomet Orthopedics, Warsaw, IN. Biomet Comprehensive Reverse Shoulder products are indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe… |
| Product code | KWS |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 21, 2013 |
| 510(k) numbers | K080642 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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