Z-0731-2020 Class III Terminated
FDA device recall Z-0731-2020 was initiated by AAP Implantate Ag on January 25, 2019 and is designated Class III. Reason for recall: Products were distributed with the incorrect instructions for use. The recall status is terminated (terminated September 30, 2024). Affected quantity: 2 units.
Recall Details
- Product Type
- Devices
- Report Date
- January 1, 2020
- Initiation Date
- January 25, 2019
- Termination Date
- September 30, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2 units
Product Description
INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453
Reason for Recall
Products were distributed with the incorrect instructions for use.
Distribution Pattern
Texas
Code Information
Lot Code: QR0013