Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, Iowa 51601
Class I - DangerousWhat Should You Do?
- Check if you have this product: LOT NO.1092045
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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
- Reason for Recall:
- Subpotent (Single Ingredient Drug): Low assay at the 6-month test 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), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, Iowa 51601
Product Codes/Lot Numbers:
LOT NO.1092045
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-1394-2012
Related Recalls
Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.