Device recall
Z-1019-2019: aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical…
FDA device recall · Class II · AAP Implantate Ag
Key facts
| Recall number (Z-number) | Z-1019-2019 |
|---|---|
| Recall event | 82159 |
| Product | aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use. |
| Product code | KDG |
| Recalling firm | AAP Implantate Ag |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 26, 2022 |
| FEI number | 3001406084 |
At a glance
- None Linked 510(k)s
- 1–9 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