3M Tekk Brand Industrial/Construction First Aid Kit, Total Resources Int'l Walnut, CA 91789

Class I - Dangerous
💊 Drugs Recalled: April 9, 2013 Total Resources Intl Other Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot 11215-05,11216-05, 11216-06, 11217-05
  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:
Total Resources Intl
Reason for Recall:
CGMP Deviations: The first aid kits that are subject to the voluntary recall is being initiated due to failure in stability testing of the active ingredient Benzalkonium Chloride.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

3M Tekk Brand Industrial/Construction First Aid Kit, Total Resources Int'l Walnut, CA 91789

Product Codes/Lot Numbers:

Lot 11215-05,11216-05, 11216-06, 11217-05

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-889-2013

Related Recalls

ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due to a Fluid Bed Drier exhaust system breach, which presents the possibility of cross-contamination where the potential contaminations are well known API's at well below efficacious dose levels.

Mar 11, 2022 Other Medical Devices Nationwide View Details →

ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due to a Fluid Bed Drier exhaust system breach, which presents the possibility of cross-contamination where the potential contaminations are well known API's at well below efficacious dose levels.

Mar 11, 2022 Other Medical Devices Nationwide View Details →