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Aesculap Implant Systems LLC recalls Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Recalled August 17, 2022 · FDA recall Z-1516-2022 · Aesculap Implant Systems
Hazard
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available: · FDA Class II
Units
5 units
Sold at
US Distribution to states of: AR, IN, NE and NC
Description
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Product
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →