🔍 RecallPedia

Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)

Class I - Dangerous
🏥 Medical Devices Recalled: March 20, 2018 Epic Extremity Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Catalog Number: 2111-0005 Lot: 51464
  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:
Epic Extremity, LLC
Reason for Recall:
There is an error in the caddy artwork that misidentifies a specific plate and screw.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)

Product Codes/Lot Numbers:

Catalog Number: 2111-0005 Lot: 51464

Distribution:

Distributed in: US, FL, PA, VA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1874-2018

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