Device recall
Z-1487-2017: MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF…
FDA device recall · Class II · Crossroads Extremity Systems Llc
Key facts
| Recall number (Z-number) | Z-1487-2017 |
|---|---|
| Recall event | 76687 |
| Product | MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R. |
| Product code | JDR |
| Recalling firm | Crossroads Extremity Systems Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 27, 2017 |
| 510(k) numbers | K142727 |
| FEI number | 3020584246 |
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