Zeiss recalls the Celldiscoverer 7 microscope's UV disinfection unit (432332-9020-000) due to potential UV radiation exposure if the unit activates outside the housing.
Under certain circumstances, the firmware makes it possible for the Disinfection unit UV (432332-9020-000) to activate outside of the Celldiscoverer 7 housing. This may result in exposure of the users to harmful UV radiation.
Zeiss is recalling the UV disinfection unit for the Celldiscoverer 7 microscope because it can activate outside the housing, exposing users to harmful UV radiation. This poses a risk of eye damage or skin injury if the unit is not properly contained.
The firmware in the UV disinfection unit can cause it to activate outside the microscope's housing under certain conditions. This exposure to UV radiation can harm the user's eyes or skin, especially if they are close to the unit during operation.
Users of the Celldiscoverer 7 microscope with the specific UV disinfection unit (432332-9020-000) are affected. Microbiologists and lab technicians using this equipment are most at risk due to potential UV exposure.
Check if your Celldiscoverer 7 microscope has the UV disinfection unit model 432332-9020-000. The unit is sold as part of the microscope system.
Ensure the UV disinfection unit is securely inside the Celldiscoverer 7 housing during use to prevent accidental activation.
No, this recall specifically applies to the UV disinfection unit model 432332-9020-000.
Look for the model number 432332-9020-000 on the UV disinfection unit for the Celldiscoverer 7 microscope.
Immediately stop using the unit and contact Zeiss for guidance, as this could expose you to harmful UV radiation.
We’ve drafted a message you can send Zeiss to request your refund or repair — edit it as you like.
Subject: Recall Z-2441-2018 — Zeiss Zeiss Hello, I own a Zeiss that is covered by recall Z-2441-2018 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.
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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.
