Device recall
Z-1161-2019: Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T
FDA device recall · Class II · Integra LifeSciences Corp.
Key facts
| Recall number (Z-number) | Z-1161-2019 |
|---|---|
| Recall event | 82377 |
| Product | Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T |
| Product code | HSN |
| Recalling firm | Integra LifeSciences Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2020 |
| 510(k) numbers | K060544, K090076, K130533 |
| FEI number | 3003418325 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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