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Upsher Smith Laboratories Recalls
6 recalls on record · January 23, 2013 to August 28, 2019 · Drugs
Recalls by year
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18
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 28, 2019DrugsFDA
Upsher Smith Laboratories, Inc. recalls Bexarotene Capsules, 75 mg, 100 capsules per bottle, Rx Only, Manufactured for: Upsher-Smith Laboratories, LLC, Maple Gr
Hazard: Failed Dissolution Specifications
October 31, 2018DrugsFDA
Upsher Smith Laboratories, Inc. recalls Bumetanide Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove,
Hazard: Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
October 31, 2018DrugsFDA
Upsher Smith Laboratories, Inc. recalls Bumetanide Tablets, USP, 1 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove,
Hazard: Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
April 30, 2014DrugsFDA
Upsher Smith Laboratories, Inc. recalls Oxandrolone Tablets, USP, 10 mg, Rx Only, C-III, 60-count bottle, Manufactured for: Upsher-Smith Labs, Minneapolis, MN 5
Hazard: Labeling: Missing Label; Three cases of product (total of 36 bottles) were packaged without the primary label on the bottle. The cases were, however, packaged in the correct finished product shipper, labeled with the correct shipper bar code label, sealed with tamper-evident tape and erroneously shipped to Upsher-Smith.
February 20, 2013DrugsFDA
Upsher Smith Laboratories, Inc. recalls Propranolol Hydrochloride Extended-release Capsules, USP, 80 mg, 100 Capsules, Rx only, Manufactured for Upsher Smith La
Hazard: Failed Dissolution Test Requirements
January 23, 2013DrugsFDA
Upsher Smith Laboratories, Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valproic Acid Activity, 100-count tablets per bottle, Rx only, Ma
Hazard: Labeling: Label Error On Declared Strength; Some bottles of product were missing the color-coded strength on the primary display panel of the label.