Device recall
Z-0110-2022: United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS…
FDA device recall · Class II · Uoc Usa Inc
Key facts
| Recall number (Z-number) | Z-0110-2022 |
|---|---|
| Recall event | 88692 |
| Product | United Orthopedics USTAR II Knee System USTAR II Knee System Segment Part, RHS, 25 mm Length, Catalog # 2915-1025 |
| Product code | KRO |
| Recalling firm | Uoc Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2023 |
| 510(k) numbers | K190100 |
| FEI number | 3009760038 |
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