Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software 1.90.2.09 or 1.90.8.06 and using...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Carl Zeiss Meditec AG directly.
Affected Products
IOLMaster 700
Quantity: 613 devices
Why Was This 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
Where Was This Sold?
This product was distributed to 38 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, IL, IN, IA, KS, LA, ME, MD, MA, MI, MS, MO, NE, NV, NH, NJ, NM, NY, NC, OH, OK, PA, SC, TX, UT, VT, VA, WA, WV, WI
About Carl Zeiss Meditec AG
Carl Zeiss Meditec AG has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report