aap Implantate AG — Class II medical device recall Z-1675-2020
Terminated recall by AAP Implantate Ag, reported 2020-04-15. The company has become aware that the soft tissue retractor is not always removed during the sawing process. T
| Recall number | Z-1675-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AAP Implantate Ag, Berlin, N/A, Germany |
| Recall initiated | 2019-11-28 |
| Classified | 2020-04-06 |
| Reported by FDA | 2020-04-15 |
| Terminated | 2025-03-27 |
| Quantity | 7 units |
| Lot numbers | I012, I025, I028 |
| Model numbers | 7971-00 |
Product
aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1675-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.