Every recall we track for Oculus Optikgeraete GMBH — 7 in all — plus the complaints and injury reports the public filed about them.
Oculus recalls Pentacam AXL Wave devices with insufficient anti-reflective coating that may cause incorrect axial length measurements. Affected units include Ref 70020, CE 0123 models sold with UDI-DI (01) 04049584025357.
Oculus recalls Myopia Master (Ref 68100) due to potential incorrect axial length measurements from insufficient anti-reflective coating. Affected units may require professional evaluation.
Oculus recalls Pentacam AXL models with insufficient anti-reflective coating that may cause incorrect axial length measurements during eye exams.
Oculus recalls Pentacam HR REF 70900 for potential inaccurate IOL alignment calculations due to software version 1.26r26 and 1.26r27. Affected devices may lead to incorrect surgical planning for toric IOLs.
Oculus recalls Pentacam AXL Wave REF 70020 devices due to software issues causing inaccurate IOL alignment calculations for toric intraocular lenses.
Oculus Optikgeraete recalls Pentacam AXL REF 70100 and HR REF 70900 ophthalmic imaging devices due to software errors affecting IOL alignment calculations.
Oculus recalls Pentacam AXL Model 70100 with specific software versions due to potential incorrect quality specification markings in eye scans. Affected units have serial numbers listed in the notice.
