Device recall
Z-1821-2022: OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF…
FDA device recall · Class II · Ossur Americas
Key facts
| Recall number (Z-number) | Z-1821-2022 |
|---|---|
| Recall event | 90775 |
| Product | OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF PKA01001T |
| Product code | ISW |
| Recalling firm | Ossur Americas |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000519909 |
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