Carl Zeiss Meditec AG recalls IOLMaster 700
Recalled Product
IOLMaster 700
Hazard / Issue
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
Issued by
FDA
Affected States: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, SC, TX, UT, VA, VT, WA, WI, WV
Lot/Code Info: Model: IOLMaster 700 Catalog Number device: 000000-1932-169
View official government recall
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