Device recall
Z-2884-2026: Brand Name: USTAR II Knee System Product Name: Hinge Box Trial, L, #1-6 and…
FDA device recall · Class II · United Orthopedic Corp.
Key facts
| Recall number (Z-number) | Z-2884-2026 |
|---|---|
| Recall event | 99026 |
| Product | Brand Name: USTAR II Knee System Product Name: Hinge Box Trial, L, #1-6 and Hinge Box Trial, R, #1-6 Model/Catalog Number: 9325-5711 thru 9325-5716 and 9325-5721 thru 9325-5726 Software Version: N/A Product Description: Knee femur prosthesis trial, reusable Component: No, N/A |
| Product code | KRO |
| Recalling firm | United Orthopedic Corp. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K190100 |
| FEI number | 1000395711 |
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