🔍 RecallPedia

Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

Class I - Dangerous
🏥 Medical Devices Recalled: January 15, 2024 D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Number: 7227.ALC; UDI/DI: 08717872031897; All lots starting with a number between 2470 and 18705.
  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:
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Reason for Recall:
When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

Product Codes/Lot Numbers:

Product Number: 7227.ALC; UDI/DI: 08717872031897; All lots starting with a number between 2470 and 18705.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1333-2024

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