Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR

Class I - Dangerous
💊 Drugs Recalled: October 29, 2012 Alara Pharmaceutical Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    11T7011A, Exp. Date: 12/2012
  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:
Alara Pharmaceutical Co
Reason for Recall:
Subpotent; 15 month stability
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR

Product Codes/Lot Numbers:

11T7011A, Exp. Date: 12/2012

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-104-2013