Showing 15,821–15,840 of 17,987 drug recalls
Drug Recall
Terminated
Historical record Class II
VERAPAMIL HCL ER, Tablet, 240 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462026001 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; VERAPAMIL HCL ER, Tablet, 240 mg may be potentially mislabeled as TRIFLUOPERAZINE HCL, Tablet, 1 mg, NDC 00781103001, Pedigree: AD52778_91, EXP: 5/21/2014. 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
FLUCONAZOLE, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462010230 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; FLUCONAZOLE, Tablet, 100 mg may be potentially mislabeled as PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: W003086, 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.
View recall →
Drug Recall
Terminated
Historical record Class II
amLODIPine BESYLATE, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68382012316 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; amLODIPine BESYLATE, Tablet, 10 mg may be potentially mislabeled as FINASTERIDE, Tablet, 5 mg, NDC 16714052201, Pedigree: AD62846_1, EXP: 2/28/2014. 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
RAMIPRIL, Capsule, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68180058901 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; RAMIPRIL, Capsule, 2.5 mg, Rx only may be potentially mislabeled as PROPAFENONE HCL, Tablet, 150 mg, NDC 00591058201, Pedigree: AD54549_13, EXP: 5/20/2014; CALCIUM POLYCARBOPHIL, Tablet, 625 mg, NDC 00536430611, Pedigree: AD73592_11, EXP: 5/31/2014. 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
IBUPROFEN, Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67877029401 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; IBUPROFEN, Tablet, 400 mg may be potentially mislabeled as ASPIRIN, Tablet, 325 mg, NDC 00536330501, Pedigree: W002573, 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.
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Drug Recall
Terminated
Historical record Class II
buPROPion HCl ER (XL), Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67767014130 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; buPROPion HCl ER (XL), Tablet, 150 mg may be potentially mislabeled as MESALAMINE CR, Capsule, 250 mg, NDC 54092018981, Pedigree: AD52412_1, EXP: 5/17/2014. 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
carBAMazepine ER, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 66993040832 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; carBAMazepine ER, Capsule, 200 mg may be potentially mislabeled as ACAMPROSATE CALCIUM DR, Tablet, 333 mg, NDC 00456333001, Pedigree: AD46333_1, EXP: 5/15/2014. 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
PHENobarbital/ HYOSCYAMINE/ ATROPINE/ SCOPOLAMINE, Tablet, 16.2 mg/0.1037 mg/0.0194 mg/0.0065 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 66213042510 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; PHENobarbital/ HYOSCYAMINE/ ATROPINE/ SCOPOLAMINE, Tablet, 16.2 mg/0.1037 mg/0.0194 mg/0.0065 mg may be potentially mislabeled as VALSARTAN, Tablet, 160 mg, NDC 00078035934, Pedigree: W003639, 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.
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Drug Recall
Terminated
Historical record Class II
IRBESARTAN, Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65862063830 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; IRBESARTAN, Tablet, 150 mg may be potentially mislabeled as ATROPINE SULFATE/DIPHENOXYLATE HCL, Tablet, 0.025 mg/2.5 mg, NDC 00378041501, Pedigree: W003597, EXP: 6/24/2014; CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: AD76686_7, EXP: 5/31/2014. 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
COLESEVELAM HCL Tablet, 625 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65597070118 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; COLESEVELAM HCL Tablet, 625 mg may be potentially mislabeled as lamoTRIgine Tablet, 50 mg (1/2 of 100 mg), NDC 13668004701, Pedigree: AD46265_31, EXP: 5/15/2014. 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
guanFACINE HCl Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162071310 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; guanFACINE HCl Tablet, 2 mg may be potentially mislabeled as buPROPion HCl ER, Tablet, 200 mg, NDC 47335073886, Pedigree: AD21790_4, EXP: 5/1/2014; AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W002997, EXP: 6/11/2014; glyBURIDE, Tablet, 1.25 mg, NDC 00093834201, Pedigree: W003677, EXP: 2/28/2014; ACYCLOVIR, Capsule, 200 mg, NDC 00093894001, Pedigree: AD60 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
FLECAINIDE ACETATE Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162064110 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; FLECAINIDE ACETATE Tablet, 50 mg may be potentially mislabeled as VITAMIN B COMPLEX W/C, Tablet, NDC 00904026013, Pedigree: AD46419_7, 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 record Class II
PROMETHAZINE HCL, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162052110 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; PROMETHAZINE HCL, Tablet, 25 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: W002574, 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
FOLIC ACID, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162036110 by Aidapak Services, LLC
Reason
Labeling:Label Mixup; FOLIC ACID, Tablet, 1 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD32328_5, EXP: 5/9/2014; DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: W003821, EXP: 6/27/2014; ATORVASTATIN CALCIUM, Tablet, 40 mg, NDC 00378212177, Pedigree: W003096, EXP: 6/13/2014. 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
RILUZOLE Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980019106 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; RILUZOLE Tablet, 50 mg may be potentially mislabeled as traZODone HCl, Tablet, 150 mg, NDC 50111044101, Pedigree: W003245, EXP: 6/17/2014. 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
DISULFIRAM Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980017101 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; DISULFIRAM Tablet, 250 mg may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00904052060, Pedigree: AD22865_22, 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 record Class II
aMILoride HCl Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980015101 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; aMILoride HCl Tablet, 5 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree: AD60272_37, EXP: 5/22/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003764, 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 record Class II
CHOLECALCIFEROL/ CALCIUM/ PHOSPHORUS Tablet, 120 units/105 mg/81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980015001 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; CHOLECALCIFEROL/CALCIUM/PHOSPHORUS Tablet, 120 units/105 mg/81 mg may be potentially mislabeled as PROMETHAZINE HCL, Tablet, 25 mg, NDC 65162052110, Pedigree: W002578, EXP: 6/3/2014; VALSARTAN, Tablet, 40 mg, NDC 00078042315, Pedigree: AD32579_1, 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 record Class II
LACTOBACILLUS Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980012950 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; LACTOBACILLUS Tablet may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 65162066850, Pedigree: AD62979_1, EXP: 5/23/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD62986_1, EXP: 5/23/2014; LITHIUM CARBONATE ER, Tablet, 225 mg (1/2 of 450 mg), NDC 00054002025, Pedigree: AD21790_25, EXP: 5/1/2014; OMEGA-3 FATTY ACID, Capsule, 100 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
COLCHICINE Tablet, 0.6 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764011907 by Aidapak Services, LLC
Reason
Labeling: Label Mixup; COLCHICINE Tablet, 0.6 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 2000 units, NDC 00904615760, Pedigree: AD46312_37, EXP: 5/16/2014; PSEUDOEPHEDRINE HCL, Tablet, 30 mg, NDC 00904505360, Pedigree: AD52993_37, EXP: 5/20/2014; SENNOSIDES, Tablet, 8.6 mg, NDC 00182109301, Pedigree: AD62992_14, EXP: 5/23/2014; CHOLECALCIFEROL, Tablet, 1000 units, NDC 00904 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 .
