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Oculus Optikgeraete Gmbh Recalls

4 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Oculus Optikgeraete Gmbh.

4Total Recalls
0Critical
712Units Affected
Aug 8, 2023Most Recent
All Recalls

Every Oculus Optikgeraete Gmbh Recall

Sorted by most recent. Click any recall for full details.

4 recalls
High RiskFDA
Oculus Optikgeraete Gmbh
Oculus Pentacam AXL , Ref 70100, CE 0123
Medical Devices·364 affected·Aug 8, 2023
High RiskFDA
Oculus Optikgeraete Gmbh
Oculus Myopia Master , Ref 68100, CE 0123
Medical Devices·173 affected·Aug 8, 2023
High RiskFDA
Oculus Optikgeraete Gmbh
Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Medical Devices·92 affected·Jul 8, 2022
High RiskFDA
Oculus Optikgeraete Gmbh
OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13. The firm name on the label is OCULUS Optikge...
Medical Implants·83 affected·Nov 21, 2017