🔍 RecallPedia

Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503; YelloPort Elite Hasson Adaptor 10mm/EA10NH. For use in laparoscopic procedures.

Class I - Dangerous
🏥 Medical Devices Recalled: January 20, 2022 Surgical Innovations Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Part/UDI-DI/Lot: ET1207503/05051986012438/735479, EA10NH/05051986012100/734029
  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:
Surgical Innovations Ltd
Reason for Recall:
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503; YelloPort Elite Hasson Adaptor 10mm/EA10NH. For use in laparoscopic procedures.

Product Codes/Lot Numbers:

Part/UDI-DI/Lot: ET1207503/05051986012438/735479, EA10NH/05051986012100/734029

Distribution:

Distributed in: US, MA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1852-2022

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