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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Levothyroxine Sodium Tablets Recalled for Subpotency

Agency Publication Date: March 24, 2026
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Summary

Macleods Pharma USA, Inc. is recalling 1,315 bottles of Levothyroxine Sodium tablets (150 mcg) because the drug is subpotent, meaning it may not contain the full amount of active medication required. This recall affects the 1,000-count bottles distributed nationwide to wholesalers and retail pharmacies. No injuries or incidents have been reported to date regarding this recall.

Risk

The drug was found to be subpotent, which means patients taking this medication may not receive the intended dose of thyroid hormone. This could lead to uncontrolled symptoms of hypothyroidism, such as fatigue, weight gain, and cold intolerance.

What You Should Do

  1. Check your prescription bottle for Levothyroxine Sodium Tablets USP 150 mcg in a 1,000-count bottle with NDC 33342-401-44.
  2. Verify if your bottle belongs to Lot 16240062A with an expiration date of 3/2026.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Macleods Pharma USA, Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Levothyroxine Sodium Tablets USP (1000 Tablets bottle)
Variants: 150 mcg, Rx Only
Lot Numbers:
16240062A (Exp 3/2026)
NDC:
33342-401-44

Manufactured by Macleods Pharmaceuticals Ltd., India

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98510
Status: Active
Manufacturer: MACLEODS PHARMA USA, INC
Sold By: Wholesalers; Retail Pharmacies
Manufactured In: India
Units Affected: 1315 bottles
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.