Reported Feb 24, 2021 · Terminated

IOLMaster 700

Carl Zeiss Meditec AG

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Carl Zeiss Meditec AG · Carl-Zeiss-Promenade 10 · Jena, N/A · N/A

Is this the product you have?

  • IOLMaster 700
Lot codes and dates
  • ModelIOLMaster 700
  • Catalog Number device000000-1932-169
Amount recalled
613 devices

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 24, 2022 · Data as of Sep 19, 4:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.