Oculus Optikgeraete Gmbh Munchholzhauser Str. 29 Wetzlar Germany
This page shows every FDA and USDA recall linked to Oculus Optikgeraete Gmbh Munchholzhauser Str. 29 Wetzlar Germany. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
7
Total Recalls
2017
First Recall
2023
Most Recent
Oculus Pentacam AXL Wave, Ref 70020, CE 0123
Aug 30, 2023
· Device
Open, Classified
Oculus Myopia Master , Ref 68100, CE 0123
Aug 30, 2023
· Device
Open, Classified
Oculus Pentacam AXL , Ref 70100, CE 0123
Aug 30, 2023
· Device
Open, Classified
Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Jul 8, 2022
· Device
Open, Classified
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Jul 8, 2022
· Device
Open, Classified
Pentacam AXL REF 70100,
Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Jul 8, 2022
· Device
Open, Classified
OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13. The firm name on...
Nov 21, 2017
· Device
Terminated