Zeiss recalls several laser scanning microscopes due to potential laser beam leakage in certain eyepiece configurations, which could exceed Class I safety limits.
In certain eyepiece configurations the laser shutter may not close completely, permitting reflected beams that may be greater than the Class I limit.
Zeiss is recalling several laser scanning microscopes because the laser shutter might not close fully in some eyepiece setups. This could allow reflected laser beams stronger than the Class I safety limit, posing a risk of eye injury during use.
In certain eyepiece configurations, the laser shutter may not close completely. This allows reflected laser beams that could exceed the Class I safety limit, potentially causing eye injury if the user looks directly into the beam.
Researchers and lab technicians using Zeiss laser scanning microscopes are most at risk. The recall affects specific models used in cell biology research.
Check for Zeiss Cell Observer SD, DirectFRAP, Laser TIRF 1, Laser TIRF 2, Laser TIRF 3, LightSheet, Elyra, or multiple Laser Scanning Microscopes. These are used in cell biology research settings.
Ensure the laser shutter closes completely in your eyepiece setup to prevent reflected beams exceeding safety limits.
Zeiss Cell Observer SD, DirectFRAP, Laser TIRF 1, Laser TIRF 2, Laser TIRF 3, LightSheet, Elyra, and multiple Laser Scanning Microscopes.
The recall does not specify a fix; users should check their eyepiece configuration to ensure the laser shutter closes completely.
Yes, if the reflected laser beams exceed the Class I safety limit, it could cause eye injury during use.
We’ve drafted a message you can send Zeiss to request your refund or repair — edit it as you like.
Subject: Recall Z-2058-2018 — Zeiss Zeiss Hello, I own a Zeiss that is covered by recall Z-2058-2018 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.
