FindMyRecallSubscribe
Class II: temporary or reversible health riskOngoing

Macleods Pharma Levothyroxine Sodium Tablets 150 mcg Recall

Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured fo…

MACLEODS PHARMA USA, INC · Princeton, NJ

Risk level
Class II
Reported by FDA
Apr 1, 2026
Recall ID
D-0403-2026
Check your lot numberHow we source this data

Summary

Macleods Pharma recalled Levothyroxine Sodium Tablets 150 mcg starting Feb 26, 2026. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0403-2026 on Apr 1, 2026. Reason: Subpotent Drug. Status: Ongoing.

Why it was recalled

Subpotent Drug

Product description

Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44

Lot numbers, UPCs & expiration codes

Lot 16240062A, exp date 3/2026

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0403-2026
Classification
Class II
Status
Ongoing
Recall initiated
Feb 26, 2026
FDA report date
Apr 1, 2026
Quantity
1315 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
MACLEODS PHARMA USA, INC

Original FDA data

Every field from FDA enforcement report D-0403-2026, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Ongoing
Country
United States
Event ID
98510
Address
103 College Rd E Fl 2
Code information
Lot 16240062A, exp date 3/2026
Postal code
08540-6611
Report date
Apr 1, 2026
Product type
Drugs
Recall number
D-0403-2026
Classification
Class II
Recalling firm
MACLEODS PHARMA USA, INC
Product quantity
1315 bottles
Reason for recall
Subpotent Drug
Voluntary / mandated
Voluntary: Firm initiated
Product description
Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc., Princeton, NJ, Manufactured by: Macleods Pharmaceuticals Ltd., Sarigam, Valsad, Guajarat, INDIA NDC 33342-401-44
Distribution pattern
Nationwide
Recall initiation date
Feb 26, 2026
Initial firm notification
Letter
Center classification date
Mar 24, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0403-2026, published Apr 1, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls