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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 741–760 of 1,000 recalls

Class IIITerminated

Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma Limited, Hyderabad, India, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 --- NDC 0409-1140-01

Hospira Inc., A Pfizer Company

Failed Impurities/Degradation Specifications; out of specification result for denitroquinoline-related impurity during three month time point

July 6, 2017 · DrugView details →
Class IIITerminated

Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5720-56

Teva Pharmaceuticals USA

Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.

June 29, 2017 · DrugView details →
Class IIITerminated

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per Bottle, Rx only, Distributed By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5721-56

Teva Pharmaceuticals USA

Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.

June 29, 2017 · DrugView details →
Class IIITerminated

Obagi-C Rx System C-Therapy Night Cream, Net wt. 2 oz. (57g) bottle, Rx only, Distributed by OMP, Inc., Long Beach, CA Made in USA, NDC 62032-222-02

Valeant Pharmaceuticals North America LLC

Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy Night Cream is being recalled due to incomplete packaging/labeling. The bottle is missing the product insert and outer carton which contain the complete instruction for use and safety information.

June 28, 2017 · DrugView details →
Class IIITerminated

Paroxetine Extended-Release Tablets USP, 12.5 mg, 30 count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland, 21202, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India, NDC: 68180-647-06

Lupin Pharmaceuticals Inc.

Failed Dissolution Specifications: out of specification observed in dissolution testing at 3 month long term stability study.

June 22, 2017 · DrugView details →
Class IIITerminated

Amitriptyline HCl Tablets, USP 25 mg, Packaged in a)100-count bottles (NDC 0781-1487-01) and b) 1000-count bottles ( NDC 0781-1487-10), Rx only, Manufactured by Sandoz Inc., Princeton, NJ 08540

Sandoz Incorporated

Cross Contamination With Other Product: Imipramine

June 16, 2017 · DrugView details →
Class IIITerminated

Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor Chewable Tablets, 80 mg & 14.2 mg, 100-count bottles, Distributed by: GlaxoSmithKline Consumer Healthcare, L.P., Moon Twp, PA 15108, UPC 3 0088-1175-47 8.

Sanofi-Aventis U.S. LLC

Superpotent Drug: high out-of-specification result for magnesium.

June 12, 2017 · DrugView details →
Class IIITerminated

Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by one paper sleeve, TOTAL 24 FL OZ (1.5 pt)(710 mL), OTC, Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015

L. Perrigo Company

Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Cough Liquid.

June 5, 2017 · DrugView details →
Class IIITerminated

G & W Clobetasol Propionate Ointment 0.05%, packaged in a) 15 g tube (NDC 0713-0656-15), b) 30 g tube (NDC 0713-0656-31, c) 45 g tube (NDC 0713-0656-37), d) 60 g tube (NDC 0713-0656-60), Rx Only, Manufactured by G & W Laboratories, Inc. 111 Coolidge Street, South Plainfield, NJ 07080

G & W Laboratories, Inc.

Failed impurities/degradation specifications: This product is being recalled due to out of specification results for Clobetasol Related Compound A, a known impurity which is a degradation product.

June 2, 2017 · DrugView details →
Class IIITerminated

BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10

Mckesson Packaging Services

Failed Moisture Limits: Product tested out-of-specification for moisture content.

May 30, 2017 · DrugView details →
Class IIITerminated

PONSTEL (Mefanamic Acid) USP, 250 mg capsules, 30-count bottles, Rx Only, Manufactured for: Shionogi Inc. Florham Park, NJ 07932 Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981

Shionogi Inc.

Failed Dissolution Specifications: Low dissolution results were obtained during stability testing

May 24, 2017 · DrugView details →
Class IIITerminated

Mefenamic Acid Capsules, USP, 250 mg, 30-count bottle, Rx only, Distributed by Prasco Laboratories, Mason, OH 45040, Manufactured by Halo Pharmaceutical Inc., Whippany, NJ 07981, NDC 66993-070-30

Shionogi Inc.

Presence of foreign substance: The recall was initiated due to black particles being observed while performing routine post-release stability testing on Mefenamic acid capsules

May 24, 2017 · DrugView details →
Class IIITerminated

Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981, NDC 66993-070-30

Shionogi Inc.

Failed Dissolution Specifications: Low dissolution results were obtained during stability testing

May 24, 2017 · DrugView details →
Class IIITerminated

Fludeoxyglucose F 18 Injection, 20mCi/mL to 200 mCi/mL at EOS, 30 mL Multiple-Dose Vial, Rx Only, Manufactured by: Lantheus MI Radiopharmaceuticals, Inc., San Juan, PR --- NDC 11994-015-01

Lantheus MI Radipharmaceuticals Inc.

Failed Impurities/Degradation Specifications; out of specification result for Acetonitrile residual solvent

May 18, 2017 · DrugView details →
Class IIITerminated

Nystatin Oral Suspension, USP, 100,000 units/mL, packaged in a) 2 fl.oz. (60mL) bottles (NDC 66689-008-02), and 500,000 units/5mL individual unit dose cup (NDC 66689-037-01) packaged in b) 50 count unit dose cups/case (NDC 66689-037-50) and c) 100 count unit dose cups/case (NDC 66689-037-99) Rx only, Manufactured by: VistaPharm, Largo, FL 33771.

VistaPharm, Inc.

Failed Impurities/Degradation Specifications: Presence of an impurity peak that exceeds approved specification.

May 17, 2017 · DrugView details →
Class IIITerminated

Benzonatate capsules, 200 mg, 100-count bottle, Rx only, Manufactured by: Strides Shasun Limited Bangaluru -560076 India, Distributed by Strides Pharma Inc East Brunswick, NJ 08816, NDC 64380-713-06

Strides Pharma INC

Failed Stability Specifications: Out of Specification results obtained for preservative Methylparaben content.

May 9, 2017 · DrugView details →
Class IIITerminated

Montelukast Sodium Oral Granules, 4 mg pouch, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-6040-93

Mylan Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications; out of specification results for Sulphoxide Impurity and Total Impurities

May 9, 2017 · DrugView details →
Class IIITerminated

HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-7785-52.

Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Superpotent Drug: above specification for the assay.

May 8, 2017 · DrugView details →
Class IIITerminated

AMLODIPINE BESYLATE TABLET, USP, 10 mg, 1000 count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013, India, Distributed by: Ascend Laboratories, LLC Montvale, NJ 07645, NDC 67877-199-10

Ascend Laboratories LLC

PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet was found co-mingled with 10 mg Amlodipine Besylate tablets in a bottle labeled as Amlodipine Besylate 10 mg.

May 5, 2017 · DrugView details →
Class IIITerminated

Famotidine for Oral Suspension USP, 40 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Goa 403 722 INDIA, NDC 68180-150-01

Lupin Pharmaceuticals Inc.

CGMP Deviations

May 2, 2017 · DrugView details →
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