Device recall
Z-2589-2011: ENDO-FUSE(TM) FUSION ROD 7 mm X 50 mm IMPLANT MATERIAL: STERILE R, Ti6A14V…
FDA device recall · Class II · Wright Medical Technology Inc
Key facts
| Recall number (Z-number) | Z-2589-2011 |
|---|---|
| Recall event | 58717 |
| Product | ENDO-FUSE(TM) FUSION ROD 7 mm X 50 mm IMPLANT MATERIAL: STERILE R, Ti6A14V, CPTi, REF: 500005950, LOT 088605355, IMPLANT MATERIAL: Wright Medical Technology, Inc , 5677 Airline Road, Arlington, TN 38002 The ENDO-FUSE(R) Intra-Osseous Fusion Rods are indicated for the reduction and fixation of… |
| Product code | HWC |
| Recalling firm | Wright Medical Technology Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 27, 2012 |
| 510(k) numbers | K051309 |
| FEI number | 1043534 |
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