Class III — AAP Implantate Ag
| Recalling firm | AAP IMPLANTATE AG |
|---|---|
| Registered facility | AAP IMPLANTATE AG (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | Products were distributed with the incorrect instructions for use. |
| Product | INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453 |
| Quantity | 2 units |
| Distribution | Texas |
| Initiated | 2019-01-25 |
| Classified | 2019-12-21 |
| Terminated | 2024-09-30 |
| Recall number | Z-0731-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — AAP Implantate Ag (Z-0731-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84383/
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