Oculus recalls Pentacam AXL models with insufficient anti-reflective coating that may cause incorrect axial length measurements during eye exams.
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Oculus is recalling Pentacam AXL devices with Ref 7010:00 and CE 0123 marking that could give wrong eye measurements. This affects eye exam accuracy and may lead to incorrect treatment decisions.
The device may have insufficient anti-reflective coating, causing inaccurate axial length measurements during eye exams. This could lead to incorrect treatment decisions for eye conditions.
Eye care professionals using the Pentacam AXL for eye exams are most affected. Patients receiving eye exams with these devices could experience incorrect treatment decisions.
Check for the model number Ref 70100 and CE 0123 marking on the device. The UDI-DI code (01) 04049584012333 is also associated with this recall.
Look for the model number Ref 70100 and CE 0123 marking on the device.
The device may have insufficient anti-reflective coating, causing incorrect axial length measurements during eye exams.
The official recall notice does not specify a remedy or action for affected devices.
The recall indicates a potential for incorrect measurements, but the official notice does not describe a risk of injury or serious harm.
We’ve drafted a message you can send Oculus to request your refund or repair — edit it as you like.
Subject: Recall Z-2483-2023 — Oculus Oculus Hello, I own a Oculus that is covered by recall Z-2483-2023 from Oculus. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.