Recall Z-1516-2022— Aesculap Implant Systems LLC
Class II · Terminated
Class II FDA medical device recall by Aesculap Implant Systems LLC, initiated 2022-07-14, terminated 2025-02-07. FDA's recall record names no specific 510(k) clearance for this event. Product: Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010. Reason: Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:.
- Recalling firm
- Aesculap Implant Systems LLC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2022-07-14
- Terminated
- 2025-02-07
- Firm location
- Center Valley, PA, United States
Product description
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Reason for recall
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Data sourced from openFDA. This site is unofficial and independent of the FDA.