Reported Sep 6, 2023 · Ongoing
Oculus Myopia Master , Ref 68100, CE 0123
Oculus Optikgeraete GmbH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Oculus Optikgeraete GMBH · Munchholzhauser Str. 29 · Wetzlar, N/A · N/A
Is this the product you have?
Oculus Myopia MasterRef 68100CE 0123
- Lot codes and dates
- UDI-DI; (01) 04049584026095
- Amount recalled
- 173 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Oculus Optikgeraete GmbH recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.