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Class II · ModerateActive recall

Losartan Potassium And Hydrochlorothiazide

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: BLK2304A, Exp. 07/31/2025
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of foreign substance: plastic-like substance.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMacleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA foreign manufacturer
Brand nameLOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Generic nameLOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Active ingredient(s)HYDROCHLOROTHIAZIDE, LOSARTAN POTASSIUM
Distributed by / forMacleods Pharma USA, Inc. Princeton, NJ 08540
NDC33342-050-44
Show the full FDA record
Full product labelLosartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, INDIA, NDC 33342-050-44
Recalling firmMACLEODS PHARMA USA, INC
DistributionUSA Nationwide
Quantity1,048 bottles
Recall initiated2024-05-07
Report date2024-05-22
Recall completed
Recall numberD-0498-2024
ClassificationClass II
FDA statusOngoing
Origin on filePrinceton NJ United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.