Zeiss recalls some Axio Observer 5 microscopes due to an incorrect Unique Device Identification label. Affected units have specific serial numbers and UDI codes. Consumers should check their product details to determine if they are impacted.
An incorrect Unique Device Identification (UDI) label was installed on some ZEISS Axio Observer 5 microscopes.
Zeiss is recalling certain Axio Observer 5 microscopes that have an incorrect Unique Device Identification (UDI) label. This issue does not pose a safety risk but requires correction to ensure proper identification and compliance with regulations.
The incorrect UDI label means the microscope may not be properly identified in regulatory or quality control systems. This could lead to mislabeling or confusion in product tracking but does not cause physical harm or injury.
Owners of Zeiss Axio Observer 5 microscopes with the specific product material number 431006-9901-000 and UDI-DI code 4064897000075 are affected. Laboratory users and customers who purchased these microscopes are most at risk of incorrect identification.
Check for the product material number 431006-9901-000 and UDI-DI code 4064897000075 on the microscope's label. The serial number should be 3859001079 for affected units.
Look for the product material number 431006-9901-000 and UDI-DI code 4064897000075 on the microscope's label.
No, the incorrect UDI label does not pose a safety risk. It only affects identification and regulatory compliance.
Check for the product material number 431006-9901-000 and UDI-DI code 4064897000075 on the label. The serial number should be 3859001079.
The recall does not require immediate action, but you should check the label to confirm if your microscope is affected.
We’ve drafted a message you can send Zeiss to request your refund or repair — edit it as you like.
Subject: Recall Z-1465-2022 — Zeiss Zeiss Hello, I own a Zeiss that is covered by recall Z-1465-2022 from Zeiss. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
