Device recall
Z-1225-2012: Smith & Nephew BIOSURE HA Interference Screw, 7 mm x 25 mm Catalog Number…
FDA device recall · Class II · Smith & Nephew, Inc. Endoscopy Division
Key facts
| Recall number (Z-number) | Z-1225-2012 |
|---|---|
| Recall event | 61138 |
| Product | Smith & Nephew BIOSURE HA Interference Screw, 7 mm x 25 mm Catalog Number: 72201772. The BIOSURE HA Interference Screw is indicated for fixation of bone-tendon-bone or soft tissue grafts during anterior/posterior cruciate ligament (ACL/PCL) reconstruction procedures. |
| Product code | HWC |
| Recalling firm | Smith & Nephew, Inc. Endoscopy Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 29, 2016 |
| 510(k) numbers | K080358 |
| FEI number | 3003604053 |
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