Oculus Optikgeraete GMBH recalls Oculus Pentacam AXL Wave, Ref 70020, CE 0123
Recalled Product
Oculus Pentacam AXL Wave, Ref 70020, CE 0123
Hazard / Issue
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI; (01) 04049584025357
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime