Oculus Pentacam AXL recall
Oculus Pentacam AXL , Ref 70100, CE 0123
Why was Oculus Pentacam AXL recalled?
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI; (01) 04049584012333
- Product
- Oculus Pentacam AXL , Ref 70100, CE 0123
- Recalling firm
- Oculus Optikgeraete GMBH
- Quantity
- 364 units
- Distribution
- US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA, TX, VA, WA. OUS: Not Provided
- Recall date
- September 6, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)