Device recall
Z-1499-2021: KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial…
FDA device recall · Class II · ConMed Corporation
Key facts
| Recall number (Z-number) | Z-1499-2021 |
|---|---|
| Recall event | 87578 |
| Product | KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE100 and KTT100. For use in open and arthroscopic procedures for knee ligament reconstruction The procedural kits have no kit specific labeling. Each product within the kits has its… |
| Product code | LXH |
| Recalling firm | ConMed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2024 |
| FEI number | 3001451571 |
At a glance
- None 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