Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Carbidopa and Levodopa Tablets Recalled by The Harvard Drug Group Due to Packaging defect: observed packaging defect, blister packaging inadequately...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact The Harvard Drug Group directly.
Affected Products
Carbidopa and Levodopa Tablets, USP 25 mg/100 mg, 10x10 Unit Dose carton, Rx Only, Manufactured in Czech Republic by: Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Manufactured for: Teva Pharmaceuticals USA, Inc. Parsippany, NJ 07054, Packaged and Distributed by: Major Pharmaceuticals Indianapolis, IN 46268 USA. NDC 0904-7257-61, UPC 3 09047 25761 4
Quantity: 17,586 cartons
Why Was This Recalled?
Packaging defect: observed packaging defect, blister packaging inadequately sealed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About The Harvard Drug Group
The Harvard Drug Group has 45 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report