Class II — AAP Implantate Ag
| Recalling firm | AAP IMPLANTATE AG |
|---|---|
| Registered facility | AAP IMPLANTATE AG (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris can develop and remain in vivo. |
| Product | aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00 |
| Quantity | 7 units |
| Distribution | Worldwide Distribution |
| Initiated | 2019-11-28 |
| Classified | 2020-04-06 |
| Terminated | 2025-03-27 |
| Recall number | Z-1675-2020 |
| 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 II recall — AAP Implantate Ag (Z-1675-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84716/
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