Aesculap recalls robotic microscopes with software 2.7 or earlier due to application errors causing rebalancing, robot recovery, and autofocus issues. Affected units have specific serial numbers and article numbers.
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Aesculap is recalling robotic microscopes with software versions 2.7 or earlier because they can cause application errors like rebalancing issues and autofocus problems. This affects specific models with known serial numbers and article numbers.
The microscope software versions 2.7 or earlier can cause application errors such as rebalancing issues, robot recovery problems, and autofocus failures. These errors may lead to incorrect use during medical procedures.
Users of the Aeos Robotic Digital Microscope with software versions 2.7 or earlier are affected. Medical professionals using these microscopes for procedures are most at risk due to potential application errors.
Check for the model name 'Aeos Robotic Digital Microscope' with software version 2.7 or earlier. Affected units have specific serial numbers: 1004, 1026, 1032, 1035, 1036, and article number PV010.
Verify the software version on your microscope; versions 2.7 or earlier are affected.
Software versions 2.7 or earlier are affected.
Affected units have serial numbers 1004, 1026, 1032, 1035, and 1036.
The recall record does not specify a remedy.
We’ve drafted a message you can send Aescul: Aesculap Implant Systems LLC to request your refund or repair — edit it as you like.
Subject: Recall Z-1516-2022 — Aescul: Aesculap Implant Systems LLC Aescul: Aesculap Implant Systems LLC Hello, I own a Aescul: Aesculap Implant Systems LLC that is covered by recall Z-1516-2022 from Aescul: Aesculap Implant Systems LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
