🔍 RecallPedia

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

Class I - Dangerous
🏥 Medical Devices Recalled: July 27, 2022 Wright Medical Technology Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot numbers 1728375 and 1728376, UDI #00840420121707.
  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:
An incorrect sizing label was applied to the carton packaging.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

Product Codes/Lot Numbers:

Lot numbers 1728375 and 1728376, UDI #00840420121707.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1567-2022

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Class I - Dangerous

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