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Carl Zeiss Meditec AG recalls ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Recalled May 4, 2022 · FDA recall Z-1007-2022 · Carl Zeiss Meditec AG
Hazard
High friction of the slider can cause the device to stick, or not move as intended. · FDA Class II
Units
1225 devices
Sold at
U.S.: AL, AR, AZ, CA, CT, FL, GA, IA, IL, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NJ, NY, OH, OR, PA, Puerto Rico, SC, TN, TX. UT, VA, WA, and WV O.U.S.: Not provided
Description
High friction of the slider can cause the device to stick, or not move as intended.
Product
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Manufacturer(s)
Carl Zeiss Meditec AG
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →