🔍 RecallPedia

ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;

Class I - Dangerous
🏥 Medical Devices Recalled: February 23, 2017 Carefusion 2200 Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Code: a.) TIN3015/ LOT 0000836578, 0000841213, 0000841215, 0000842719, 0000842721, 0000845423, 0000848061, 0000849715, 0000850938, 0000852076, 0000854859; Product Code: b.) TIN3018/ LOT 0000836574, 0000841212, 0000852078
  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:
Carefusion 2200 Inc
Reason for Recall:
The integrity of the sterile packaging is potentially compromised.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;

Product Codes/Lot Numbers:

Product Code: a.) TIN3015/ LOT 0000836578, 0000841213, 0000841215, 0000842719, 0000842721, 0000845423, 0000848061, 0000849715, 0000850938, 0000852076, 0000854859; Product Code: b.) TIN3018/ LOT 0000836574, 0000841212, 0000852078

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1423-2018

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