Quick Facts at a Glance
- Recall Date
- July 13, 2026
- Hazard Level
- HIGH
- Brands
- LEVOTHYROXINE SODIUM, Major Pharmaceuticals
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- LEVOTHYROXINE SODIUM, Major Pharmaceuticals
- Model numbers
- Lot #: N02266, Exp. Date 11/2026
- UPC codes
- 0904-6949, 0904-6950, 0904-6951, 0904-6952, 0904-6953, 0904-6954, 0904-6955, 0904-6956 +10 more
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
July 13, 2026
Reported by FDA DRUG
July 29, 2026
RecallRadar source check
August 4, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Subpotent Drug
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Major Pharmaceuticals or your healthcare provider for guidance. Notification method: Letter
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Full Description
Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6955-61. Generic: LEVOTHYROXINE SODIUM; Brand: LEVOTHYROXINE SODIUM. Reason: Subpotent Drug. Classification: Class II. Quantity: N/A. Distribution: Nationwide in the USA.
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: How to Get Refunds and ReplacementsWant to Know First?
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