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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 661–680 of 1,000 recalls

Class IIITerminated

BuPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150 mg, a) 30 count (NDC 59746- 758-30) & b) 90 count (NDC 59746-758-90) bottles, Rx only, Manufactured b Jubilant Generis Ltd, Roorkee, India, Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD

Jubilant Cadista Pharmaceuticals, Inc.

Failed Dissolution Specifications; 9-monthstability timepoint

February 28, 2019 · DrugView details →
Class IIITerminated

Moxifloxacin Ophthalmic Solution USP, 0.5%, 3 mL bottle, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, INDIA, NDC 68180-422-01.

Lupin Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: Expansion of July 2018 and February 2019 recall due to high out-of-specification for impurities.

February 26, 2019 · DrugView details →
Class IIITerminated

Oxybutynin Chloride, Extended-Release Tablets USP, 10 mg, 100 Tablet, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19154 NDC: 62175-271-37

Lannett Company Inc.

Failed Dissolution Specifications

February 21, 2019 · DrugView details →
Class IIITerminated

Temozolomide Capsules, 5 mg, packaged in a) 5-count bottle (NDC 43975-252-05) b) 14-count bottle (NDC 43975-252-14), Rx only, Mfd. by: Stason Pharmaceuticals, Inc., Irvine, CA 92618, Dist. By: Amerigen Pharmaceuticals, Lyndhurst, NJ 07071

Amerigen Pharmaceuticals Inc.

Failed dissolution specifications

February 19, 2019 · DrugView details →
Class IIITerminated

Lovastatin Tablets USP, 40 mg, packaged in a) 100-count bottles (NDC 68001-316-00) and b)1000-count bottles (NDC 68001-316-08), Rx Only, Manufactured by: Lupin Limited, Goa 403 722 INDIA For BluePoint Laboratories.

American Health Packaging

CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.

February 19, 2019 · DrugView details →
Class IIITerminated

Ciclopirox shampoo 1%,120 mL bottle, Rx only, Manufactured By Perrigo Bronx, NY 10457 Distributed by Perrigo Allegan, MI 49010, 45802-401-09

Perrigo New York, Inc.

Failed Degradation/Impurities Specifications: Out of specification related substance results during stability testing.

February 13, 2019 · DrugView details →
Class IIITerminated

Diltiazem HCl Extended-Release Capsules, USP 180mg, Packaged in a) 100-count bottles (NDC 0378-5280-01), and b) 500-count bottles (NDC 0378-5280-05), Rx only, Manufactured by: Mylan Pharmaceuticals Inc. Morgantown, WV, 26505

Mylan Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: High out of specification results obtained during routine stability testing

February 13, 2019 · DrugView details →
Class IIITerminated

Lovastatin Tablets USP, 40 mg, packaged in a) 60-count (NDC 68180-469-07 and b) 100-count (NDC 68180-469-01) bottles, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Goa 403 722 INDIA.

Lupin Pharmaceuticals Inc.

CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.

February 13, 2019 · DrugView details →
Class IIITerminated

Mometasone Furoate Cream, 0.1%, 45 g tube, Rx Only, Manufactured by: G&W Laboratories, Inc. South Plainfield, NJ 07080, NDC 0713-0726-37

ACP Nimble Buyer, Inc.

Labeling: Not Elsewhere Classified. Mometasone Furoate Cream has an NDC typographical error.

February 7, 2019 · DrugView details →
Class IIITerminated

Oxytocin 20 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1002 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-703-99.

Advanced Pharma Inc.

Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

February 6, 2019 · DrugView details →
Class IIITerminated

Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.

Advanced Pharma Inc.

Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

February 6, 2019 · DrugView details →
Class IIITerminated

Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.

Advanced Pharma Inc.

Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.

February 6, 2019 · DrugView details →
Class IIITerminated

Esomeprazole Magnesium Delayed-Release Capsules USP, 40mg*, a) 90-count bottle (NDC 43598-510-90) b) 1000 count bottle (NDC 43598-510-10), Rx only, Mfd By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 INDIA.

Dr. Reddy's Laboratories, Inc.

Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown pellets.

February 6, 2019 · DrugView details →
Class IIITerminated

Moxifloxacin Ophthalmic Solution USP, 0.5%, 3 mL dropper bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 Manufactured by: lupin Limited Pithampur (M.P.) 454 775 India. NDC 68180-422-01

Lupin Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: Out of specification test results in related substance at three-month long term stability study was obtained.

February 1, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 120 mg, packaged in a) 30-count bottles (NDC 0187-0795-30); and b) 90-count bottles (NDC 0187-0795-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Diltiazem HCl CD capsules, 360 mg, 90-count bottles, Rx Only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; NDC 68682-521-01.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 300 mg, packaged in a) 30-count bottles (NDC 0187-0798-30); and b) 90-count bottles (NDC 0187-0798-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 180 mg, packaged in a) 30-count bottles (NDC 0187-0796-30); and b) 90-count bottles (NDC 0187-0796-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Cardizem CD (diltiazem HCl) capsules, 240 mg, packaged in a) 30-count bottles (NDC 0187-0797-30); and b) 90-count bottles (NDC 0187-0797-42), Rx Only, Manufactured for: Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7, Canada.

Valeant Pharmaceuticals North America LLC

Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.

January 30, 2019 · DrugView details →
Class IIITerminated

Bimatoprost Ophthalmic Solution 0.03%, packaged in a) 5 mL (NDC 68180-429-02) and b) 7.5 mL (NDC 68180-429-03) bottles, Rx only, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, INDIA.

Lupin Pharmaceuticals Inc.

Failed Impurities/Degradation Specifications: OOS results observed in any other individual impurity and total impurities.

January 28, 2019 · DrugView details →
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