🔍 RecallPedia

Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212

Class I - Dangerous
🏥 Medical Devices Recalled: July 9, 2015 Cadence Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Packged Lots: Catalog Number 5202: 79713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W006324/5; Catalog Number 5205: 79748-03; Catalog Number 5212: W008136/1, W008686/1, W011240/1, W010905/1, W012135/1, W014053/1, W015838/1, W011240
  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:
Cadence Inc.
Reason for Recall:
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212

Product Codes/Lot Numbers:

Packged Lots: Catalog Number 5202: 79713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W006324/5; Catalog Number 5205: 79748-03; Catalog Number 5212: W008136/1, W008686/1, W011240/1, W010905/1, W012135/1, W014053/1, W015838/1, W011240

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2364-2015

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