Skip to main content
Get Alerts

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.

Filters
Recall details
Location
Date range
Clear filters

Showing 16,041–16,060 of 17,987 drug recalls

Drug Recall Terminated Historical recordClass II

ISOSORBIDE MONONITRATE ER Tablet, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175012837

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ISOSORBIDE MONONITRATE ER Tablet, 30 mg may be potentially mislabeled as LOSARTAN POTASSIUM, Tablet, 25 mg, NDC 16714058102, Pedigree: W003899, EXP: 6/27/2014; MISOPROSTOL, Tablet, 100 mcg, NDC 43386016012, Pedigree: AD42611_7, EXP: 5/14/2014; hydrOXYzine PAMOATE, Capsule, 100 mg, NDC 00555032402, Pedigree: W003332, EXP: 6/18/2014; glyBURIDE, Tablet, 2.5 mg, NDC 0009383
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

ISOSORBIDE MONONITRATE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175010601

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ISOSORBIDE MONONITRATE Tablet, 10 mg may be potentially mislabeled as ASCORBIC ACID, Tablet, 250 mg, NDC 00904052260, Pedigree: AD28322_10, EXP: 5/6/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

ESTERIFIED ESTROGENS Tablet, 0.625 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 61570007301

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ESTERIFIED ESTROGENS, Tablet, 0.625 mg may be potentially mislabeled as ETODOLAC, Tablet, 400 mg, NDC 51672401801, Pedigree: W003734, EXP: 6/26/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

OLANZAPINE, Tablet 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505311203

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; OLANZAPINE, Tablet 7.5 mg may be potentially mislabeled as NORTRIPTYLINE HCL, Capsule, 75 mg, NDC 00093081301, Pedigree: AD21790_73, EXP: 5/1/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

ATORVASTATIN CALCIUM Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505257909

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ATORVASTATIN CALCIUM Tablet, 20 mg may be potentially mislabeled as guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003850, EXP: 6/27/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

CILOSTAZOL Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505252201

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

MAGNESIUM GLUCONATE DIHYDRATE Tablet, 500 mg (27 mg Elemental Magnesium), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258017201

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; MAGNESIUM GLUCONATE DIHYDRATE Tablet, 500 mg (27 mg Elemental Magnesium) may be potentially mislabeled as hydrALAZINE HCl, Tablet, 100 mg, NDC 23155000401, Pedigree: AD30197_7, EXP: 5/9/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258016001

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00378180701, Pedigree: AD73652_10, EXP: 5/30/2014; HYOSCYAMINE SULFATE ER, Tablet, 0.375 mg, NDC 43199001401, Pedigree: W003576, EXP: 6/24/2014; MELATONIN, Tablet, 3 mg, NDC 51991001406, Pedigree: AD70655_14, EXP: 5/28/2014; MELATONIN, Tablet, 3 mg, NDC
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

ASCORBIC ACID Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258014101

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ASCORBIC ACID Tablet, 500 mg may be potentially mislabeled as FEBUXOSTAT, Tablet, 40 mg, NDC 64764091830, Pedigree: AD23082_16, EXP: 11/1/2013.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

ZINC SULFATE Capsule, 220 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258013101

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ZINC SULFATE Capsule, 220 mg may be potentially mislabeled as CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD52778_10, EXP: 5/20/2014; CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: W003638, EXP: 6/25/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

medroxyPROGESTERone ACETATE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762374202

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; medroxyPROGESTERone ACETATE, Tablet, 10 mg may be potentially mislabeled as hydrALAZINE HCl, Tablet, 100 mg, NDC 23155000401, Pedigree: AD46312_13, EXP: 5/16/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

NIFEdipine Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762100401

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; NIFEdipine, Capsule, 10 mg may be potentially mislabeled as NITROFURANTOIN MONOHYDRATE/ MACROCRYSTALS, Capsule, 100 mg, NDC 47781030301, Pedigree: AD52778_58, EXP: 5/20/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

COLESTIPOL HCL MICRONIZED Tablet, 1 g, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762045001

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; COLESTIPOL HCL MICRONIZED Tablet, 1 g may be potentially mislabeled as rifAXIMin, Tablet, 200 mg, NDC 65649030103, Pedigree: AD54587_10, EXP: 4/30/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

methylPREDNISolone Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59746000103

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; methylPREDNISolone Tablet, 4 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 137 mcg, NDC 00781519192, Pedigree: AD22616_10, EXP: 5/2/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

DARUNAVIR Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59676056630

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; DARUNAVIR Tablet, 800 mg may be potentially mislabeled as HYDROcodone BITARTRATE/ ACETAMINOPHEN, Tablet, 7.5 mg/325 mg, NDC 52544016201, Pedigree: W004005, EXP: 7/1/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

ARIPiprazole Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59148000613

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; ARIPiprazole Tablet, 2 mg may be potentially mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: AD21790_40, EXP: 5/1/2014; ATOMOXETINE HCL, Capsule, 80 mg, NDC 00002325030, Pedigree: AD30140_19, EXP: 5/7/2014; OLANZapine, Tablet, 7.5 mg, NDC 55111016530, Pedigree: AD46265_46, EXP: 5/15/2014; REPAGLINIDE, Tablet, 2 mg, NDC 00169008481, Pedigree: AD464
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

SEVELAMER HCl Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 58468002101

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; SEVELAMER HCl Tablet, 800 mg may be potentially mislabeled as RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: W002857, EXP: 6/7/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

CITALOPRAM Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050788

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; CITALOPRAM Tablet, 10 mg may be potentially mislabeled as OXYBUTYNIN CHLORIDE, Tablet, 5 mg, NDC 00603497521, Pedigree: AD52778_61, EXP: 5/20/2014; COENZYME Q-10, Capsule, 30 mg, NDC 00904501546, Pedigree: W002814, EXP: 6/7/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

METOPROLOL TARTRATE Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050652

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; METOPROLOL TARTRATE, Tablet, 25 mg may be potentially mislabeled as ASCORBIC ACID, Tablet, 250 mg, NDC 00904052260, Pedigree: W003826, EXP: 6/27/2014; amLODIPine BESYLATE, Tablet, 5 mg, NDC 00093716798, Pedigree: W002840, EXP: 6/7/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

View recall →

Drug Recall Terminated Historical recordClass II

METOPROLOL TARTRATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050652

by Aidapak Services, LLC

Reason
Labeling:Label Mixup; METOPROLOL TARTRATE Tablet, 12.5 mg (1/2 of 25 mg) may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00904789159, Pedigree: AD68022_1, EXP: 5/28/2014; METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg), NDC 57664050652, Pedigree: AD68010_14, EXP: 5/28/2014.
Recall initiated
July 2, 2013
Reported by FDA
January 22, 2014
Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

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.