Device recall
Z-1816-2013: Synthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number…
FDA device recall · Class II · Synthes USA HQ, Inc.
Key facts
| Recall number (Z-number) | Z-1816-2013 |
|---|---|
| Recall event | 65669 |
| Product | Synthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number 390.007, Lot Number 6800599 Synthes Large External Fixation is intended for use to provide treatment for long bone and pelvic fractures that require external fixation. |
| Product code | KTT |
| Recalling firm | Synthes USA HQ, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K082650 |
| FEI number | 3005180112 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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