Torsemide Tablets recalled over manufacturing violations
- Recall date
- December 14, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Apotex Corp. recalls Torsemide Tablets, 5 mg 100-count bottle, Rx only ,Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9W, 6Y3, Ma…
- Recall number
- D-0245-2017
- FDA classification
- Class II
- Brand / firm
- Apotex Corp.
- Sold / distributed
- United States
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Torsemide Tablets, 5 mg 100-count bottle, Rx only ,Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9W, 6Y3, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-0232-01
Get recall alerts
Free email alert whenever Apotex Corp. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Apotex Corp.