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Oculus Optikgeraete GMBH recalls Oculus Myopia Master , Ref 68100, CE 0123
Recalled September 6, 2023 · FDA recall Z-2484-2023 · Oculus Optikgeraete
Hazard
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements. · FDA Class II
Units
173 units
Sold at
US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA, TX, VA, WA. OUS: Not Provided
Description
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Product
Oculus Myopia Master , Ref 68100, CE 0123
Manufacturer(s)
Oculus Optikgeraete GMBH
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →