Showing 16,021–16,040 of 17,987 drug recalls
Drug Recall
Terminated
Historical record Class II
QUEtiapine FUMARATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65862048901 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; QUEtiapine FUMARATE, Tablet, 25 mg may be potentially mislabeled as chlordiazePOXIDE HCl, Capsule, 25 mg, NDC 00555015902, Pedigree: AD49426_1, 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.
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Drug Recall
Terminated
Historical record Class II
rifAXIMin Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65649030103 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; rifAXIMin Tablet, 200 mg may be potentially mislabeled as CapsuleTOPRIL, Tablet, 25 mg, NDC 00143117201, Pedigree: AD52778_19, 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.
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Drug Recall
Terminated
Historical record Class II
BENAZEPRIL HCL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075410 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 40 mg may be potentially mislabeled as NEFAZODONE HCL, Tablet, 200 mg, NDC 00093102506, Pedigree: AD46414_44, EXP: 5/16/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003931, EXP: 6/28/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD42592_1, EXP: 5/14/2014; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/25 Recall initiated
July 2, 2013 Reported by FDA
January 22, 2014 Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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Drug Recall
Terminated
Historical record Class II
BENAZEPRIL HCL Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075110 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 5 mg may be potentially mislabeled as ZINC SULFATE, Capsule, 220 mg, NDC 60258013101, Pedigree: AD52993_34, 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.
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Drug Recall
Terminated
Historical record Class II
MULTIVITAMIN/MULTIMINERAL Tablet, Distributed by: AidaPak Service, LLC, NDC 65162066850 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL Tablet may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD62865_13, EXP: 5/23/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003514, EXP: 6/21/2014. 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 record Class II
MULTIVITAMIN/MULTIMINERAL Tablet, Distributed by: AidaPak Service, LLC, NDC 65162066810 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL Tablet may be potentially mislabeled as PRENATAL MULTIVITAMIN/MULTIMINERAL Tablet, NDC 00904531360, Pedigree: AD73652_16, EXP: 5/30/2014. Recall initiated
July 2, 2013 Reported by FDA
January 22, 2014 Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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Drug Recall
Terminated
Historical record Class II
SODIUM BICARBONATE Tablet, 650 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980018210 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; SODIUM BICARBONATE Tablet, 650 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 00135051001, Pedigree: W002974, EXP: 6/11/2014. Recall initiated
July 2, 2013 Reported by FDA
January 22, 2014 Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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Drug Recall
Terminated
Historical record Class II
PHOSPHORUS Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980010401 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; PHOSPHORUS Tablet, 250 mg may be potentially mislabeled as CITALOPRAM, Tablet, 10 mg, NDC 57664050788, Pedigree: AD56921_1, EXP: 5/21/2014; VENLAFAXINE HCL, Tablet, 75 mg, NDC 00093738201, Pedigree: W002533, EXP: 2/28/2014; NITROFURANTOIN MACROCRYSTALS, Capsule, 50 mg, NDC 47781030701, Pedigree: AD25452_4, EXP: 5/3/2014; traZODone HCl, Tablet, 50 mg, NDC 50111043303, P Recall initiated
July 2, 2013 Reported by FDA
January 22, 2014 Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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Drug Recall
Terminated
Historical record Class II
FEBUXOSTAT Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764091830 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; FEBUXOSTAT Tablet, 40 mg may be potentially mislabeled as methylPREDNISolone, Tablet, 4 mg, NDC 59746000103, Pedigree: AD21811_17, EXP: 5/1/2014; tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: W002663, EXP: 6/5/2014; SODIUM CHLORIDE, Tablet, 1000 mg, NDC 00527111610, Pedigree: W003926, 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.
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Drug Recall
Terminated
Historical record Class II
LUBIPROSTONE Capsule, 24 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764024060 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; LUBIPROSTONE Capsule, 24 mcg may be potentially mislabeled as ARIPiprazole, Tablet, 2 mg, NDC 59148000613, Pedigree: AD21790_43, EXP: 5/1/2014; CYANOCOBALAMIN, Tablet, 1000 mcg, NDC 00904421713, Pedigree: AD21846_46, EXP: 5/1/2014; VALSARTAN, Tablet, 160 mg, NDC 00078035934, Pedigree: AD39858_1, 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.
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Drug Recall
Terminated
Historical record Class II
HYDROCORTISONE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64720033105 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; HYDROCORTISONE Tablet, 5 mg may be potentially mislabeled as ORPHENADRINE CITRATE ER, Tablet, 100 mg, NDC 43386048024, Pedigree: W002962, EXP: 6/11/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: W003045, EXP: 6/12/2014. Recall initiated
July 2, 2013 Reported by FDA
January 22, 2014 Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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Drug Recall
Terminated
Historical record Class II
LISINOPRIL Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679092701 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; LISINOPRIL Tablet, 2.5 mg may be potentially mislabeled as RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: AD23087_1, EXP: 5/2/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: W003358, EXP: 6/19/2014. 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 record Class II
PANTOPRAZOLE SODIUM DR Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679043304 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; PANTOPRAZOLE SODIUM DR Tablet, 20 mg may be potentially mislabeled as FOSINOPRIL SODIUM, Tablet, 20 mg, NDC 60505251102, Pedigree: AD70690_1, EXP: 5/29/2014. Recall initiated
July 2, 2013 Reported by FDA
January 22, 2014 Distribution
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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Drug Recall
Terminated
Historical record Class II
MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64376081601 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 112 mcg, NDC 00527134601, Pedigree: AD60272_22, EXP: 5/22/2014; ATORVASTATIN CALCIUM, Tablet, 80 mg, NDC 00378212277, Pedigree: AD73627_1, EXP: 5/30/2014; MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 37205018581, Pedigree: W002513, EXP: 6/3/2014. 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 record Class II
BENZOCAINE/MENTHOL, Lozenge, 15 mg/2.6 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824073116 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; BENZOCAINE/MENTHOL Lozenge, 15 mg/2.6 mg may be potentially mislabeled as CHOLECALCIFEROL/ CALCIUM/ PHOSPHORUS, Tablet, 120 units/105 mg/81 mg, NDC 64980015001, Pedigree: AD32345_1, EXP: 5/14/2014. 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 record Class II
guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000834 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: AD62829_18, EXP: 5/24/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: AD62834_4, EXP: 5/24/2014; diphenhydrAMINE HCl, Tablet, 25 mg, NDC 00904555159, Pedigree: W003513, EXP: 6/21/2014; DOCUSATE SODIUM, Capsule, 250 mg, 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 record Class II
guaiFENesin ER, Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000815 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as MISOPROSTOL, Tablet, 200 mcg, NDC 59762500801, Pedigree: AD21965_13, EXP: 5/1/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: AD56917_7, EXP: 5/21/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD73627_17, EXP: 5/30/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: W003216 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 record Class II
METOPROLOL TARTRATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 63304057901 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg) may be potentially mislabeled as PIOGLITAZONE, Tablet, 15 mg, NDC 00591320530, Pedigree: AD22845_1, EXP: 4/30/2014; LEVOTHYROXINE SODIUM, Tablet, 12.5 mcg (1/2 of 25 mcg), NDC 00527134101, Pedigree: AD73525_49, EXP: 5/30/2014. 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 record Class II
OXcarbazepine Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018588 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; OXcarbazepine Tablet, 600 mg may be potentially mislabeled as LACTASE ENZYME, Tablet, 3000 units, NDC 24385014976, Pedigree: AD30028_25, EXP: 5/7/2014. 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 record Class II
OXcarbazepine Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018388 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; OXcarbazepine Tablet, 150 mg may be potentially mislabeled as traZODone HCl, Tablet, 50 mg, NDC 50111043301, Pedigree: AD54562_1, 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 →
Data last updated: October 2, 2026 ET
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 .
