Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract Recalled by Carl Zeiss Meditec AG Due to High friction of the slider can cause the...
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
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Quantity: 1225 devices
Why Was This Recalled?
High friction of the slider can cause the device to stick, or not move as intended.
Where Was This Sold?
This product was distributed to 31 states: AL, AZ, AR, CA, CT, FL, GA, IL, IA, KS, LA, MD, MA, MI, MN, MS, MO, MT, NJ, NY, NC, OH, OR, PA, SC, TN, TX, UT, VA, WA, WV
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