FDAFDA · Food and drugs·Recall number D-0498-2024
Losartan 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
Published May 22, 2024 · Recall initiated: May 7, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of foreign substance: plastic-like substance.
What to do
Voluntary: Firm initiated
Recall details
- Brand
- LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
- Manufacturer
- MACLEODS PHARMA USA, INC
- Distributor
- USA Nationwide
- UPC
- 0333342051448
- Lot
- Lot #: BLK2304A, Exp. 07/31/2025
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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