The Recall Desk

FDA (Drugs) recall action 65690

Aidapak Services, LLC recalled 265 products on 2014-01-29

The FDA (Drugs) publishes a recall like this one as 265 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 265 pages.

Products
265
Announced
2014-01-29
Critical
0
Units
134,998

Why these products were recalled

Labeling: Label Mixup: SENNOSIDES, Tablet, 8.6 mg may have potentially been mislabeled as one of the following drugs: FEXOFENADINE HCL, Tablet, 180 mg, NDC 41167412003, Pedigree: AD62834_1, EXP: 5/23/2014; TRIMETHOBENZAMIDE HCL, Capsule, 300 mg, NDC 53489037601, Pedigree: W002976, EXP: 6/11/2014; LORATADINE, Tablet, 10 mg, NDC 45802065078, Pedigree: W003253, EXP: 6/17/2014.

Labeling: Label Mixup: LEVOTHYROXINE SODIUM, Tablet, 137 mcg may have potentially been mislabeled as the following drug: ISONIAZID, Tablet, 300 mg, NDC 00555007102, Pedigree: AD60272_70, EXP: 5/22/2014.

Labeling: Label Mixup: PANTOPRAZOLE SODIUM DR, Tablet, 20 mg may be potentially mislabeled as one of the following drugs: HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, NDC 00574025001, Pedigree: AD60272_16, EXP: 5/22/2014; MULTIVITAMIN/MULTIMINERAL, Tablet, 0 mg, NDC 65162066810, Pedigree: AD73646_13, EXP: 5/30/2014.

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

26–50 of 265

  • ModerateFDA (Drugs)··2014-01-29

    Fosinopril Sodium Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling 10 mg Fosinopril Sodium tablets that may be mislabeled as Mercaptopurine 50 mg.

    Product
    FOSINOPRIL SODIUM, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00185004109.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Lithium Carbonate ER Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Lithium Carbonate ER tablets due to a labeling error where they may be mislabeled as other medications.

    Product
    LITHIUM CARBONATE ER, Tablet, 225 mg (1/2 of 450 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00054002025.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Imipramine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Imipramine HCL 25 mg tablets because they may have been mislabeled as Fenofibrate 54 mg.

    Product
    IMIPRAMINE HCL, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781176401.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Dicyclomine HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Dicyclomine HCL 20 mg tablets because they may have been mislabeled as Ramipril 2.5 mg capsules.

    Product
    DICYCLOMINE HCL, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591079501.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Propranolol HCL ER Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Propranolol HCL ER capsules because they may have been mislabeled as Cinacalcet HCL tablets.

    Product
    PROPRANOLOL HCL ER, Capsule, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00228277811.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Valsartan Tablets Recalled for Potential Labeling Mixup with Other Drugs

    Aidapak Services is recalling Valsartan 160 mg tablets because they may have been mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    VALSARTAN, Tablet, 160 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00078035934.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls CapsuleTOPRIL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling CapsuleTOPRIL 6.25 mg tablets because they may have been mislabeled as Lubiprostone 24 mcg capsules.

    Product
    CapsuleTOPRIL, Tablet, 6.25 mg (1/2 of 12.5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00143117101.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Niacin TR Capsules Due to Potential Label Mixup

    Aidapak Services is recalling Niacin TR capsules because they may have been mislabeled as other drugs like Perphenazine or Melatonin.

    Product
    NIACIN TR, Capsule, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00904063160.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Oxybutynin Chloride Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Oxybutynin Chloride tablets that may be mislabeled as Pimozide. The error could lead to patients receiving the wrong medication.

    Product
    OXYBUTYNIN CHLORIDE, Tablet, 2.5 mg (1/2 of 5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00603497521
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Venlafaxine HCL ER Capsules Recalled for Potential Label Mixup

    Aidapak Services is recalling Venlafaxine HCL ER capsules due to a potential label mixup with other medications. The repacked drugs were distributed in four western states.

    Product
    VENLAFAXINE HCL ER, Capsule, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093738656.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    Entecavir Tablets Recalled Due to Potential Label Mixup

    Aidapak Services is recalling Entecavir tablets because they may be mislabeled as other prescription drugs.

    Product
    ENTECAVIR, Tablet, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00003161112.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    Methazolamide Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Methazolamide tablets that may have been mislabeled as Buprenorphine HCL due to a label mixup.

    Product
    METHAZOLAMIDE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781107101.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Nicotine Polacrilex Lozenges Due to Potential Labeling Errors

    Aidapak Services is recalling 2 mg nicotine polacrilex lozenges because they may have been mislabeled as other prescription drugs. The affected products were distributed in four western states.

    Product
    NICOTINE POLACRILEX, LOZENGE, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00135051001.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls MEXILETINE HCL Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling MEXILETINE HCL capsules because they may have been mislabeled as CALCIUM ACETATE. The error could lead to patients receiving the wrong medication.

    Product
    MEXILETINE HCL, Capsule, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093873901.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Acyclovir Tablets Recalled Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Acyclovir 800 mg tablets that may have been mislabeled as Pantoprazole Sodium 20 mg.

    Product
    ACYCLOVIR, Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093894701.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Carbamazepine ER Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling carbamazepine ER tablets that may be mislabeled as isosorbide dinitrate or sirolimus.

    Product
    carBAMazepine ER, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00078051005.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Chlorthalidone Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Chlorthalidone 12.5 mg tablets because they may have been mislabeled as Propranolol HCl 5 mg tablets.

    Product
    CHLORTHALIDONE, Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00378022201.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Pregabalin Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Pregabalin 25 mg capsules because they may have been mislabeled as Cholecalciferol or Glyburide.

    Product
    PREGABALIN, Capsule, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00071101268.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Irbesartan Tablets Due to Potential Labeling Error

    Aidapak Services is recalling 150 mg Irbesartan tablets because they may have been mislabeled as Benazepril HCl 40 mg.

    Product
    IRBESARTAN, Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093746556.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Estradiol Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Estradiol 0.5 mg tablets because they may have been mislabeled as Nicotine Polacrilex gum.

    Product
    ESTRADIOL, Tablet, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00555089902.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Carvedilol Phosphate ER Capsules Recalled for Potential Labeling Error

    Aidapak Services is recalling Carvedilol Phosphate ER capsules due to a potential label mixup with Bumetanide tablets.

    Product
    CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00007337113.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Levothyroxine Sodium Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Levothyroxine Sodium tablets that may have been mislabeled as Pramipexole Di-HCl.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 175 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378181701
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Hyoscyamine Sulfate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Hyoscyamine Sulfate ODT tablets that may have been mislabeled as Fluoxetine HCl capsules.

    Product
    HYOSCYAMINE SULFATE ODT, Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574024701.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Perphenazine Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 16 mg Perphenazine tablets because they may have been mislabeled as other prescription drugs.

    Product
    PERPHENAZINE, Tablet, 16 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781104901.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    FDA Recalls Lithium Carbonate ER Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Lithium Carbonate ER tablets because they may be mislabeled as Vitamin B Complex Prolonged Release tablets.

    Product
    LITHIUM CARBONATE ER, Tablet, 300 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054002125.
    Category
    Distribution
    4 states