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Beaver Visitec International, Inc. recalls CustomEyes kits
Recalled March 8, 2023 · FDA recall Z-1200-2023 · Beaver Visitec International
Hazard
Device packaging may contain open seals, compromising product sterility. · FDA Class II
Units
4640 units in total
Sold at
US distribution in AL, CA, CO, DC, FL, GA, IL, LA, MD, MN, MT, NC, NH, NJ, NM, NY, OH OK, PA, RI, TN, TX, UT, VA, VT, WA, and WI OUS distribution to Canada, Japan, and South Africa
Description
Device packaging may contain open seals, compromising product sterility.
Product
CustomEyes kits
Manufacturer(s)
Beaver Visitec International, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →