Recalls / Active ingredient / Bumetanide
Bumetanide
3 FDA drug recalls involving the active ingredient “Bumetanide”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2018-09-19 | Class II | Bumetanide Tablets, USP, 1 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Map | Upsher Smith Laboratories, Inc. |
| 2018-09-19 | Class II | Bumetanide Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Map | Upsher Smith Laboratories, Inc. |
| 2013-11-06 | Class III | Bumetanide Tablets USP 0.5 mg. Rx Only, a) 100-count Bottle, b) 500-count Bottle, Sandoz Inc., Princeton, NJ 0 | Sandoz Inc |