FDA Device recall Z-0732-2020
INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425
- FDA Device
- Class III
- terminated
- Published 2020-01-01
On 2020-01-01 the FDA classified a Class III recall of INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425 by Aap Implantate Ag, citing products were distributed with the incorrect instructions for use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0732-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-01-25 |
| Published | 2020-01-01 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Aap Implantate Ag |
| Distribution | TX |
Product
INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425
Reason
Products were distributed with the incorrect instructions for use.
Identifiers
| code_info | Lot Code: QS0007 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0732-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.