Carl Zeiss Meditec recalls IOLMaster 700 devices with specific software versions due to potential patient data mismatch during patient list selection. Affected units may need software update or correction.
When using software 1.90.2.09 or 1.90.8.06 and using modality worklist functionality for patient data transfer, the selection of the patient in the patient list may not match the patient information displayed on the right side of the screen
Carl Zeiss Meditec is recalling IOLMaster 700 devices that have software versions 1.90.2.09 or 1.90.8.06. This could cause patient information displayed on the screen to not match the selected patient in the list, which might lead to incorrect patient data being used in eye measurements.
The software issue can cause the patient selected in the list to not match the patient information shown on the screen. This mismatch might result in incorrect eye measurement data being recorded, potentially affecting treatment decisions.
Ophthalmologists and eye care professionals using the IOLMaster 700 with specific software versions are most at risk. Patients using the device for eye measurements may also be affected if the software error occurs.
Check for the IOLMaster 700 device with software versions 1.90.2.09 or 1.90.8.06. The catalog number is 000000-1932-169.
Verify the software version on your IOLMaster 700 device. If it is 1.90.2.09 or 1.90.8.06, it is affected.
Software versions 1.90.2.09 and 1.90.8.06 are affected.
Check the software version on your IOLMaster 700 device. If it is 1.90.2.09 or 1.90.8.06, it is affected.
The recall record does not specify a remedy, so contact Carl Zeiss Meditec for guidance.
We’ve drafted a message you can send Carl Zeiss Meditec to request your refund or repair — edit it as you like.
Subject: Recall Z-1133-2021 — Carl Zeiss Meditec Carl Zeiss Meditec Hello, I own a Carl Zeiss Meditec that is covered by recall Z-1133-2021 from Carl Zeiss Meditec. 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.
