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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 8,681–8,700 of 17,964 drug recalls

Drug Recall Terminated Historical recordClass III

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.

by Valeant Pharmaceuticals North America LLC

Reason
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Recall initiated
January 30, 2019
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass III

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.

by Valeant Pharmaceuticals North America LLC

Reason
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Recall initiated
January 30, 2019
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass III

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.

by Valeant Pharmaceuticals North America LLC

Reason
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Recall initiated
January 30, 2019
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass III

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.

by Valeant Pharmaceuticals North America LLC

Reason
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Recall initiated
January 30, 2019
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass III

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.

by Valeant Pharmaceuticals North America LLC

Reason
Failed Dissolution Specifications: high out of specification results for dissolution when measuring the amount of drug released at certain time points.
Recall initiated
January 30, 2019
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass III

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

by Lupin Pharmaceuticals Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification test results in related substance at three-month long term stability study was obtained.
Recall initiated
February 1, 2019
Reported by FDA
February 20, 2019
Distribution
Product was distributed by 5 wholesalers, 6 drug chains, 4 mail order pharmacies and 1 mail order pharmacy/supermarket who may have further distribute the product throughout the United States.

View recall →

Drug Recall Terminated Historical recordClass III

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

by Akorn Inc

Reason
Failed Stability Specifications: out of specification results for opalescence at 7 month stability study.
Recall initiated
December 20, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass II

LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.

by US Compounding Inc

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: Labels are missing lot and expiration date and are printed as Lot# YYYDDYY@XX with a Beyond Use Date: MM/DD/YYY.
Recall initiated
January 24, 2019
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Folic Acid, 5mg/ml injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Zinc Sulfate,10mg/ml injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Glycyrrhizic Acid, 8mg/mL Injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Dexpanthenol, 250mg/mL Injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Lysine HCl, 100 mg/mL injection, 10ml, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Leucine/Isoleucine/Valine injection, 10mg/10mg/5mg/mL/mL, 10mL vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Pyridoxine HCl, 100 mg/mL Injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Procaine HCl, 2% injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Trim Calm, GABA/Magnesium/Taurine/Theanine, 50mg/50mg/50mg/50mg/ml, 10mL vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Folic Acid, Injection, 10 mg/mL, 10mL vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Zinc Sulfate, 5mg/mL injection, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

Myer's Cocktail, Pyridoxine/Dexpanthenol/Calcium Gluconate/Niacinamide/Vit B6/Vit B1/Leucine/Vit B5/Riboflavin/Ascorbic Acid/Hydroxycobalamin/Magnesium Chloride, 10ml vial, Rx Only, Promise Pharmacy Compounding Specialists 31818 US Hwy 19N, Palm Harbor, FL 34684

by Promise Pharmacy, LLC

Reason
Lack of sterility assurance.
Recall initiated
December 17, 2018
Reported by FDA
February 20, 2019
Distribution
Nationwide in the USA.

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.