Oculus Optikgeraete GMBH recalls

7 recalls on record · latest: August 8, 2023

Official U.S. recall history for Oculus Optikgeraete GMBH, compiled from official government records.

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Oculus Optikgeraete GMBH recalls Oculus Pentacam AXL , Ref 70100, CE 0123

August 8, 2023 · Medical device recalls Moderate risk Their is a potential that optical devices with insufficient anti-reflective coa…

Oculus Optikgeraete GMBH recalls Oculus Myopia Master , Ref 68100, CE 0123

August 8, 2023 · Medical device recalls Moderate risk Their is a potential that optical devices with insufficient anti-reflective coa…

Oculus Optikgeraete GMBH recalls Oculus Pentacam AXL Wave, Ref 70020, CE 0123

August 8, 2023 · Medical device recalls Moderate risk Their is a potential that optical devices with insufficient anti-reflective coa…

Oculus Optikgeraete GMBH recalls Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.

July 8, 2022 · Medical device recalls Moderate risk Due to a software issue, IOL calculator printout often does not accurately refl…

Oculus Optikgeraete GMBH recalls Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

July 8, 2022 · Medical device recalls Moderate risk Due to a software issue, IOL calculator printout often does not accurately refl…

Oculus Optikgeraete GMBH recalls Pentacam HR REF 70900. Used to image the anterior segment of the eye.

July 8, 2022 · Medical device recalls Moderate risk Due to a software issue, IOL calculator printout often does not accurately refl…

Oculus Optikgeraete GMBH recalls OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13. The firm name on the label…

November 21, 2017 · Medical device recalls Moderate risk The device software versions have an anomaly which may produce an erroneous mar…