The Recall Desk
HighFDA (Drugs)·D-0710-2026·Announced 2026-07-29

Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns

Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (125 mcg) because the medication may be subpotent.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is for a subpotent drug, which poses a risk of harm because the patient may not receive the required dose of medication.

Plain-English summary

Major Pharmaceuticals has initiated a voluntary recall of Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg). The affected product is packaged in 10-tablet unit dose blisters per carton and is distributed nationwide in the USA.

The recall was initiated because the medication may be subpotent, meaning it may not contain the intended amount of the active ingredient.

Consumers should contact their healthcare provider or pharmacist regarding the use of this medication. Specific lot information includes Bag lot numbers N02266A and N02266, and Blister lot number N02266, all with an expiration date of 11/2026.

The recalled product

Product
LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Brand
LEVOTHYROXINE SODIUM
Manufacturer
Major Pharmaceuticals
Hazard
  • subpotent-drug

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Bag lot #: N02266A
  • N02266B
  • Exp. Date 11/2026
  • Blister lot #: N02266

UPCs (1)

  • 0055154356305

Distribution

Distributed nationwide across the United States.