Roxane Laboratories, Inc. recalls Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-4…
- Recall date
- December 22, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0437-2017
- FDA classification
- Class II
- Brand / firm
- Roxane Laboratories, Inc.
- Sold / distributed
- Nationwide in the USA
Why it was recalled
Failed Tablet/Capsule Specifications: An unusually thick tablet was reported through a complaint.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Furosemide Tablets USP, 20 mg, 1000 count bottles, Rx only, Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-4297-31.
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