Oculus Optikgeraete GMBH recalls Oculus Pentacam AXL , Ref 70100, CE 0123
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Read the official notice →- Date
- 2023-09-06
- Country
- United States
- Brand
- Oculus Optikgeraete
- Product
- Oculus Pentacam AXL , Ref 70100, CE 0123
- Classification
- Class II
- Units
- US Nationwide distribution in the states of CA, FL, MA, MN, NY, NC, OH, PA,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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