Device recall
Z-1232-2012: REF 905570 3.5 mm Lactoscrew Anchor Size 2 white Maxbraid,(Lactosorb L-15…
FDA device recall · Class II · Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-1232-2012 |
|---|---|
| Recall event | 61104 |
| Product | REF 905570 3.5 mm Lactoscrew Anchor Size 2 white Maxbraid ,(Lactosorb L-15 resorbable copolymer ) Sterile, EO; Biomet Sports Medicine, Warsaw, IN Product Usage: The Biomet Sports Medicine Soft Tissue Anchoring Devices are resorbable repair devices used to attach soft tissue to bone. |
| Product code | HWC |
| Recalling firm | Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 12, 2013 |
| 510(k) numbers | K080088 |
| FEI number | 1825034 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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