🔍 RecallPedia

Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical instrument used on the AEGIS Anterior Lumbar Plate System.

Class I - Dangerous
🏥 Medical Devices Recalled: November 20, 2015 DePuy Spine Surgical Instruments

What Should You Do?

  1. Check if you have this product:
    LOT NUMBER: GB0906 GB0707 GB0907 GB58815 GB59244 GB61134
  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:
DePuy Spine, Inc.
Reason for Recall:
Manufacturing error within the Torque Handle may prohibit some handles from being able to fully assemble with the tightener shaft. The design of the inspection gage does not account for the additional shift length
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical instrument used on the AEGIS Anterior Lumbar Plate System.

Product Codes/Lot Numbers:

LOT NUMBER: GB0906 GB0707 GB0907 GB58815 GB59244 GB61134

Distribution:

Distributed in: US, NC, MI, CO, MD, FL, ID, TX, CA, NY

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0454-2016

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