Oculus Optikgeraete recalls

Oculus Optikgeraete appears in 7 official U.S. recall notices indexed by RecallRadar, most recently on 2023-09-06.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Oculus Myopia Master , Ref 68100, CE 0123
  FDA Device · Class II · 2023-09-06 · Oculus Optikgeraete
• Oculus Pentacam AXL Wave, Ref 70020, CE 0123
  FDA Device · Class II · 2023-09-06 · Oculus Optikgeraete
• Oculus Pentacam AXL , Ref 70100, CE 0123
  FDA Device · Class II · 2023-09-06 · Oculus Optikgeraete
• Pentacam HR REF 70900
  FDA Device · Class II · 2022-09-07 · Oculus Optikgeraete
• Pentacam AXL REF 70100, Pentacam HR REF 70900
  FDA Device · Class II · 2022-09-07 · Oculus Optikgeraete
• Pentacam AXL Wave REF 70020
  FDA Device · Class II · 2022-09-07 · Oculus Optikgeraete
• OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13
  FDA Device · Class II · 2018-02-28 · Oculus Optikgeraete