Oculus Pentacam AXL , Ref 70100, CE 0123 recall — FDA Z-2483-2023
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Overview of recall records associated with Oculus Optikgeraete GMBH, including dates, categories and classifications where available.
Classification mix: Class II: 6.
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs
Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs
Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs
This page summarizes recall records in which the official source identifies Oculus Optikgeraete GMBH as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.