🔍 RecallPedia

Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Class I - Dangerous
💊 Drugs Recalled: July 25, 2012 Lloyd Inc. of Iowa Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot 1093992 and 1094095, exp. date 9/2012
  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:
Lloyd Inc. of Iowa
Reason for Recall:
Subpotent; 9-month stability interval
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Product Codes/Lot Numbers:

Lot 1093992 and 1094095, exp. date 9/2012

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-101-2013

Related Recalls