FDA recall Z-0731-2020
AAP Implantate Ag · Class III · device
Product
INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453
Reason for recall
Products were distributed with the incorrect instructions for use.
Distribution
Texas
Key facts
- Status
- Terminated
- Initiation date
- 2019-01-25
- Report date
- 2020-01-01
- Termination date
- 2024-09-30
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Berlin, Germany
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0731-2020