INTEGRA — Class III medical device recall Z-0732-2020
Terminated recall by AAP Implantate Ag, reported 2020-01-01, distributed in TX. Products were distributed with the incorrect instructions for use.
| Recall number | Z-0732-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | AAP Implantate Ag, Berlin, Germany |
| Recall initiated | 2019-01-25 |
| Classified | 2019-12-21 |
| Reported by FDA | 2020-01-01 |
| Terminated | 2024-09-30 |
| Distributed | TX |
| Quantity | 7 units |
| Lot numbers | QS0007 |
| Model numbers | 430425 |
Product
INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425
Reason for recall
Products were distributed with the incorrect instructions for use.
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-0732-2020. 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.