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Beaver Visitec International, Inc. recalls Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to be used to aid in cataract, corneal, or refractive su
Recalled December 29, 2021 · FDA recall Z-0406-2022 · Beaver Visitec International
Hazard
Kit packaging may have small holes compromising product sterility · FDA Class II
Units
380 units
Sold at
CA, CO, LA, MA, MD, ND, PA, TN, UT
Description
Kit packaging may have small holes compromising product sterility
Product
Malosa Core Suface Treatment Pack -Medical Corneal Kit intended to be used to aid in cataract, corneal, or refractive surgery. Part Number: MMK110/3
Manufacturer(s)
Beaver Visitec International, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →