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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 14841–14860 of 17,832 recalls

Class IITerminated

Captomer [succinic acid (from 100 mg DMSA)] capsules, 65 mg, 45-count bottles, Manufactured By: Thorne Research, Inc., P.O. Box 25, Dover, Idaho 83825, UPC 6 93749 74002 5

Thorne Research Inc

Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are marketed as dietary supplements and labeled to be sourced from Dimercaptosuccinic Acid (DMSA) which is the active ingredient in an FDA approved drug making these products unapproved new drugs.

June 12, 2014 · DrugView details →
Class IITerminated

Heparin Sodium in 5% Dextrose Injection, Heparin, 25,000 USP Heparin Units/250 mL (100 USP Heparin Units/mL), 250 mL, Single-Dose Container, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7793-62

Hospira Inc.

Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking from primary container of bag.

June 6, 2014 · DrugView details →
Class IIITerminated

DENBLAN Anticavity Fluoride Toothpaste, Whitening formula, sodium monofluorophosphate 0.76%, 2.6 oz/75 mL tube, Laboratories Darphin, Dist, Paris France

Estee Lauder Inc

Stability Data Does Not Support Expiry

June 6, 2014 · DrugView details →
Class IITerminated

Carbidopa and Levodopa Tablets USP, 25mg/100mg, 1000 count bottle, Rx only, Manufactured in Israel by Teva Pharmaceutical IND, LTD., Jeruselem, Israel, for Teva Pharmaceuticals USA, Sellersville, PA, NDC 0093-0293-10

Teva Pharmaceuticals USA

Failed Tablet/Capsule Specifications: Teva is recalling one lot of Carbidopa and Levodopa Tablets USP, 25mg/100mg due to the potential for superpotent tablets.

June 5, 2014 · DrugView details →
Class IIITerminated

APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 522 mg, a) 7-count HDPE bottle (NDC 0024-5812-07), b) 30-count HDPE bottle (NDC 0024-5812-30), Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7

Valeant Pharmaceuticals North America LLC

Labeling: Incorrect or Missing Package Insert

June 5, 2014 · DrugView details →
Class IIITerminated

APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 348 mg, a) 7-count HDPE bottle (NDC 0024-5811-07), b) 30-count HDPE bottle (NDC 0024-5811-30), Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7

Valeant Pharmaceuticals North America LLC

Labeling: Incorrect or Missing Package Insert

June 5, 2014 · DrugView details →
Class IIITerminated

APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 174 mg, 7-count HDPE bottle, Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7, NDC 0024-5810-07.

Valeant Pharmaceuticals North America LLC

Labeling: Incorrect or Missing Package Insert

June 5, 2014 · DrugView details →
Class IITerminated

Atorvastatin Calcium 40 MG Tablet, MFG: Apotex NDC# 6050525808

Unit Dose Solutions Inc

Presence of Foreign Tablets/Capsules:179 doses of Valacyclovir HCl 500 mg tablets were repacked in unit dose packslabeled as Atorvastatin Calcium

June 2, 2014 · DrugView details →
Class ITerminated

Soliris (eculizumab), 300 mg/30 mL (10 mg/mL), 30 mL Single-Use Vial, Rx only, Manufactured by: Alexion Pharmaceuticals, Inc., Cheshire, CT 06410, NDC 25682-001-01, UPC 3 25682-001-01 6.

Alexion Pharmaceuticals, Inc.

Presence of Particulate Matter: Product failed the appearance for the presence of visible particles under labeled storage condition.

June 2, 2014 · DrugView details →
Class IITerminated

Diphenhydramine (Alcohol Base) 25 mg / 0.5 mL Solution, 30 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

Brookfield Prescription Center Inc. dba MD Custom Rx

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

May 30, 2014 · DrugView details →
Class IITerminated

HCG 125U/Tab Tablet Tritu, 50 tablets per bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

Brookfield Prescription Center Inc. dba MD Custom Rx

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

May 30, 2014 · DrugView details →
Class IITerminated

HCG (Human Chorionic Gonadotropin) 125 units/ 0.1 mL drop, 5 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

Brookfield Prescription Center Inc. dba MD Custom Rx

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

May 30, 2014 · DrugView details →
Class IITerminated

Mometasone 0.6 mg /60 mL Irrigation solution, 4000 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

Brookfield Prescription Center Inc. dba MD Custom Rx

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

May 30, 2014 · DrugView details →
Class IITerminated

HCG (Human Chorionic Gonadotropin) + Methylcobalamin (Methyl B12), 1500 units + 1000 mcg/mL drop, 8 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

Brookfield Prescription Center Inc. dba MD Custom Rx

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

May 30, 2014 · DrugView details →
Class IITerminated

HCG (Human Chorionic Gonadotropin) 200 units/ 0.1 mL drops, packaged in 5 mL and 10 mL bottles, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

Brookfield Prescription Center Inc. dba MD Custom Rx

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

May 30, 2014 · DrugView details →
Class IITerminated

Fluvastatin Capsules USP, 20 mg, Rx Only, 30-count bottle, manufactured for Teva Pharmaceuticals, Sellersville, PA, by Teva Pharmaceutical IND LTD, Jerusalem, Israel, NDC 0093-7442-56

Teva Pharmaceuticals USA

Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Fluvastatin Capsules USP, 20 mg due to a customer complaint trend regarding capsule breakage.

May 29, 2014 · DrugView details →
Class IIITerminated

Foradil Aerolizer (formoterol fumarate inhalation powder), 12 mcg per capsule, 60 Capsules, Rx only, Manufactured for: Merck, Sharpe & Dohne Corp., a subsidiary of Merck & Co., Inc. Whitehouse Station, NJ 08889, Manufactured by: Novartis Pharma AG Basle, Switzerland NDC 0085-1401-01

Novartis Pharmaceuticals Corp.

Failed Stability Specification; out of specification result for particle size distribution during stability testing

May 28, 2014 · DrugView details →
Class ITerminated

del Nido Cardioplegia with Lidocaine 1052.8 ml, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Central Admixture Pharmacy Services, Inc.

Non Sterility; microbial contamination identified as Aspergillus species

May 28, 2014 · DrugView details →
Class ITerminated

adenosine 90 mg in 0.9% sodium chloride/90 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Central Admixture Pharmacy Services, Inc.

Non Sterility; microbial contamination identified as Aspergillus species

May 28, 2014 · DrugView details →
Class ITerminated

PEDIATRIC CARDIOPLEGIA, 255 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150

Central Admixture Pharmacy Services, Inc.

Non Sterility; microbial contamination identified as Aspergillus species

May 28, 2014 · DrugView details →
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