Civic Data
FDA RecallsUSDA RecallsAbout

FDA Recalls

  • Food recalls
  • Drug recalls
  • Device recalls

USDA Recalls

  • All USDA recalls
  • Poultry recalls
  • Meat recalls
  • Egg recalls

About

  • About us
  • FDA guides
  • USDA guides
  • Data sources
  • Privacy policy

Data

  • OpenFDA API
  • USDA FSIS

© 2026Civic Data · Data sourced from OpenFDA and USDA FSIS · Not affiliated with the U.S. Food and Drug Administration or the U.S. Department of Agriculture · Always verify against official sources before acting

  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 501–520 of 1,000 recalls

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 →
Class IIITerminated

Clobetasol Propionate Emollient Cream 0.05%, a) 30 gram (NDC 50383-270-30) and b) 60 gram (NDC 50383-270-60) tubes, Rx only. Manufacturer: Akorn Inc. 369 Bayview Ave., Amityville, NY 117701.

Akorn Inc

Failed Stability Specification; out of specification (OOS) results for a preservative at 9 month stability study.

January 25, 2019 · DrugView details →
Class IIITerminated

Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufacturer: Macleods Pharmaceuticals Ltd Al Oxalis Labs Baddi Himachal Pradesh INDIA, UPC Code 33342032186 ---- NDC 33342-321-86

Oxalis Labs

Defective Container; complaints of leakage.

January 11, 2019 · DrugView details →
Class IIITerminated

LOPERAMIDE HCL TABLETS USP, 2 mg, ANTI-DIARRHEAL, 24 caplets per carton, OTC, Distributed by Drug Mart-Food Fair Medina Ohio 44256 Ohm Laboratories Inc. UPC 0 93351 11270 6 NDC#:53943-123-24

Sun Pharmaceutical Industries, Inc.

Labeling Not Elsewhere Classified: The front panel indicates 24 caplets whereas the side panel indicates 12 caplets. The drug product carton contains 24 caplets.

December 26, 2018 · DrugView details →
Class IIITerminated

COSOPT Ophthalmic Solution, USP, (2% Dorzolamide Hydrochloride, 0.5% Timolol Maleate), 10 mL dropper bottle, Sterile, Rx only, Distributed by: Akorn, Inc., Lake Forest, IL, NDC: 17478-605-10

Akorn Inc

Failed Stability Specifications: out of specification results for opalescence at 7 month stability study.

December 20, 2018 · DrugView details →
← PreviousPage 26 of 50Next →