🔍 RecallPedia

Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to a conventional technique for total knee replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.t Tibial Trial Handle

Class I - Dangerous
🏥 Medical Devices Recalled: June 23, 2017 Exactech Implants & Prosthetics

What Should You Do?

  1. Check if you have this product:
    Catalog Number 02-029-29-1000, Lot Number 83843-001.
  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:
Exactech, Inc.
Reason for Recall:
The Truliant Tibial Trial Handle's pin may disassociate from the main body.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Truliant Tibial Trial Handle. To assist the surgeon in the implantation of Truliant Knee system components according to a conventional technique for total knee replacement. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.t Tibial Trial Handle

Product Codes/Lot Numbers:

Catalog Number 02-029-29-1000, Lot Number 83843-001.

Distribution:

Distributed in: US, AZ, CA, CO, FL, IL, OH, OK, NV, NY, SC, TN

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-3018-2017

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