FDAFDA · Food and drugs·Recall number D-0437-2017
Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-4297-31.
Published February 1, 2017 · Recall initiated: December 22, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- FUROSEMIDE
- Manufacturer
- Roxane Laboratories, Inc.
- Distributor
- Nationwide in the USA
- UPC
- 0300544301251
- Lot
- Lot# 660833A, Exp 08/31/18
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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