🔍 RecallPedia

Oculus Myopia Master , Ref 68100, CE 0123

Class I - Dangerous
🏥 Medical Devices Recalled: August 8, 2023 Oculus Optikgeraete GMBH Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI; (01) 04049584026095
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Oculus Optikgeraete GMBH
Reason for Recall:
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Oculus Myopia Master , Ref 68100, CE 0123

Product Codes/Lot Numbers:

UDI-DI; (01) 04049584026095

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2484-2023

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