Recall Z-0731-2020— AAP Implantate Ag
Class III · Terminated
Class III FDA medical device recall by AAP Implantate Ag, initiated 2019-01-25, terminated 2024-09-30. FDA's recall record names no specific 510(k) clearance for this event. Product: INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453. Reason: Products were distributed with the incorrect instructions for use..
- Recalling firm
- AAP Implantate Ag
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2019-01-25
- Terminated
- 2024-09-30
- Firm location
- Berlin, Germany
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.