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  1. FDA Recalls
  2. ›Drug Recalls

FDA Drug Recalls

Recalls of prescription drugs, over-the-counter medications, and compounded pharmaceuticals.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 5861–5880 of 17,773 recalls

Class IITerminated

Unasyn (ampicillin sodium/sulbacatam) for injection, 1.5 g* per vial, Rx Only, 10 vials/carton, Made in Italy Distributed by Roerig Division of Pfizer Inc. New York, NY 10017 vial NDC 0049-0013-81, carton NDC 0049-0013-83

Pfizer Inc.

Presence of Particulate Matter: particulate matter identified after reconstitution.

May 29, 2020 · DrugView details →
Class IIOngoing

amneal Metformin Hydrochloride Extended-release Tablets, USP, 500 mg Rx Only, 500 Tablets bottles, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad 388213, INDIA Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 65162-178-50

Amneal Pharmaceuticals of New York, LLC

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

May 29, 2020 · DrugView details →
Class IIITerminated

Lamotrigine Tablets, USP, 150 mg, Rx Only, a) 60 count Bottle, NDC 42291-368-60, b) 500 count Bottle, NDC 42291-368-50, Manufactured for: AvKARE, Inc. Pulaski, TN 38478.

AVKARE Inc.

Presence of Foreign Substance consistent with granules from desiccant packs used during storage

May 28, 2020 · DrugView details →
Class IITerminated

Gaviscon Regular Strength Liquid Antacid Cool Mint, 12 FL OZ (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-41

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

May 28, 2020 · DrugView details →
Class IITerminated

Gaviscon Extra Strength Liquid Antacid Extra Strength Cherry, 12 FL OZ. (355 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0574-41

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

May 28, 2020 · DrugView details →
Class IITerminated

oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 888-339-0874, NDC 70092-1068-07

QuVa Pharma, Inc.

Subpotent drug - Product did not contain drug.

May 28, 2020 · DrugView details →
Class IITerminated

Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Nagpur - 441 108, India, NDC 68180-513-03.

Lupin Pharmaceuticals Inc.

Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.

May 28, 2020 · DrugView details →
Class IITerminated

Gaviscon Liquid Antacid Extra Strength, Cool Mint, 12 FL OZ (355 mL) single pack and twin pack, Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0095-41

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

May 28, 2020 · DrugView details →
Class IITerminated

Gaviscon Regular Strength Liquid Antacid Cool Mint, 6 FL OZ (177 mL), Distributed by: GSK Consumer Healthcare Warren, NJ 07059, NDC 0135-0094-42

Glaxosmithkline Consumer Healthcare Holdings

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

May 28, 2020 · DrugView details →
Class IIITerminated

Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg, packaged in 2 blister cards containing 15 tablets each (30 tablets), Rx Only, Distributed by Wyeth Pharmaceuticals LLC A subsidiary of Pfizer In Philadelphia, PA 19101 Made in Ireland, NDC 00008-1123-12

Pfizer Inc.

Failed Dissolution Specifications

May 27, 2020 · DrugView details →
Class IICompleted

Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326 NDC 60505-0260-1

Apotex Inc.

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels

May 27, 2020 · DrugView details →
Class IIITerminated

Olanzapine Tablets, USP 7.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810, NDC 66993-682-30

Aurobindo Pharma USA Inc.

Failed Impurities/ Degradation Specifications

May 26, 2020 · DrugView details →
Class IIITerminated

Clonidine Hydrochloride Tablets, USP 0.1 mg 100-count bottles, Rx only, Manufactured by: Unichem Laboratories LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Manufactured for : Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ 08816, NDC 29300-135-01

UNICHEM PHARMACEUTICALS USA INC

Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container.

May 26, 2020 · DrugView details →
Class IIITerminated

Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx only, Manufactured for: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Aurolife Pharma LLC Dayton, NJ 08810, NDC 66993-680-30

Aurobindo Pharma USA Inc.

Failed Impurities/ Degradation Specifications

May 26, 2020 · DrugView details →
Class IIITerminated

Lamotrigine Tablets, USP, 150 mg, 20,000-count bulk container, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA, For repackaging by: AvKare Inc., Pulaski, TN 38478, Bulk Shipment, NDC 59746-247-97.

Jubilant Cadista Pharmaceuticals, Inc.

Presence of Foreign Substance visually consistent with the silica granules present in the desiccant packs utilized during storage of the product.

May 26, 2020 · DrugView details →
Class IITerminated

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 5 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0971-02

Teva Pharmaceuticals USA

Some bottles may contain mixed strengths of the product.

May 22, 2020 · DrugView details →
Class ITerminated

NP Thyroid 60, Thyroid Tablets, USP, 1 grain (60 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-330-01.

Acella Pharmaceuticals, LLC

Superpotent Drug.

May 22, 2020 · DrugView details →
Class IITerminated

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 15 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0777-02

Teva Pharmaceuticals USA

Some bottles may contain mixed strengths of the product.

May 22, 2020 · DrugView details →
Class IITerminated

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed Amphetamine Salts Product), 20 mg, 100 count bottles, Rx Only, Teva Pharmaceuticals USA, INC. North Wales, PA 19454, NDC 0555-0973-02

Teva Pharmaceuticals USA

Some bottles may contain mixed strengths of the product.

May 22, 2020 · DrugView details →
Class ITerminated

NP Thyroid 30, Thyroid Tablets, USP, 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured For: Acella Pharmaceuticals, LLC, Alpharetta, GA 30005, NDC 42192-329-01.

Acella Pharmaceuticals, LLC

Superpotent Drug.

May 22, 2020 · DrugView details →
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