Device recall
Z-1126-2019: ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the…
FDA device recall · Class II · ulrich medical USA Inc
Key facts
| Recall number (Z-number) | Z-1126-2019 |
|---|---|
| Recall event | 82497 |
| Product | ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal implant construct. |
| Product code | LXL |
| Recalling firm | ulrich medical USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 10, 2020 |
| 510(k) numbers | K102853, K123717 |
| FEI number | 3005532635 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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