Device recall
Z-0580-2016: CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Knee…
FDA device recall · Class II · Corflex
Key facts
| Recall number (Z-number) | Z-0580-2016 |
|---|---|
| Recall event | 72727 |
| Product | CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee… |
| Product code | ITQ |
| Recalling firm | Corflex |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2016 |
| FEI number | 1218997 |
At a glance
- None 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