🔍 RecallPedia

INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS

Class I - Dangerous
🏥 Medical Devices Recalled: November 4, 2021 Wright Medical Technology Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model 220223214E, Lot Code 06113718691661809 (GTIN: 00840420125033)
  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:
Wright Medical Technology Inc
Reason for Recall:
The package contents and package labeling do not match.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS

Product Codes/Lot Numbers:

Model 220223214E, Lot Code 06113718691661809 (GTIN: 00840420125033)

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0316-2022

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stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty

Wright Medical Technology

Class I - Dangerous

Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.

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