🔍 RecallPedia

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left

Class I - Dangerous
🏥 Medical Devices Recalled: March 18, 2021 Waldemar Link GmbH & Co. KG (Mfg Site) Implants & Prosthetics

What Should You Do?

  1. Check if you have this product:
    Item No. 15-2979/02; UDI-DI: 04026575328109.
  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:
Waldemar Link GmbH & Co. KG (Mfg Site)
Reason for Recall:
The firm discovered through customer complaints that device segments may not meet specifications.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

LINK Endo-Model Modular Knee Prosthesis System Femoral Segment, Size 4, Left

Product Codes/Lot Numbers:

Item No. 15-2979/02; UDI-DI: 04026575328109.

Distribution:

Distributed in: AL, GA, IL, IN, KS, NJ, NY, TX

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2049-2023

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Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

Waldemar Link GmbH & Co. KG (Mfg Site)

Class I - Dangerous

The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

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