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

1–25 of 265

  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Sennosides Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Sennosides tablets because they may have been mislabeled as other medications. The recall covers distribution in four western states.

    Product
    SENNOSIDES, Tablet, 8.6 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00182109301.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Levothyroxine Sodium Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Levothyroxine Sodium tablets that may have been mislabeled as Isoniazid due to a labeling error.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 137 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00527163801.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Mislabeled Pantoprazole Sodium DR Tablets

    Aidapak Services is recalling 20 mg Pantoprazole Sodium DR tablets because they may be mislabeled as Hyoscyamine Sulfate or Multivitamin/Multimineral.

    Product
    PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00008060601.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Nifedipine ER Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Nifedipine ER 60 mg tablets because they may have been mislabeled as Nicotine Polacrilex 2 mg lozenges.

    Product
    NIFEdipine ER, Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591319401.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Simvastatin Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Simvastatin 40 mg tablets because they may have been mislabeled as Metoprolol Tartrate 12.5 mg.

    Product
    SIMVASTATIN, Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093715598.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Nebivolol Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Nebivolol HCL 5 mg tablets because they may have been mislabeled as Thyroid or Rasagiline Mesylate.

    Product
    NEBIVOLOL HCL, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00456140530.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Levothyroxine Sodium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Levothyroxine Sodium tablets because they may have been mislabeled as other prescription drugs.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 12.5 mcg (1/2 of 25 mcg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00527134101.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Tri-Buffered Aspirin Tablets Due to Labeling Error

    Aidapak Services is recalling Tri-Buffered Aspirin tablets because they may have been mislabeled as a different medication. The error involves a potential mix-up with Isometheptene Mucate/Dichlorphenazone/APAP capsules.

    Product
    TRI-BUFFERED ASPIRIN, Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904201559.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    FDA Recalls Mislabeled Tacrolimus Capsules Distributed by Aidapak Services

    Aidapak Services is recalling 1 mg tacrolimus capsules that may have been mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    TACROLIMUS, Capsule, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781210301.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    Aidapak Recalls Guanfacine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling guanfacine HCl tablets because they may have been mislabeled as other prescription drugs.

    Product
    guanFACINE HCl, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591044401.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    SitaGLIPtin Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling sitaGLIPtin phosphate tablets because they may be mislabeled as Lactobacillus or Cyanocobalamin.

    Product
    sitaGLIPtin PHOSPHATE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00006011231.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    FDA Recalls Levothyroxine Sodium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Levothyroxine Sodium tablets that may have been mislabeled as Omega-3 Fatty Acid capsules.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 137 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781519192.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Pregabalin Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Pregabalin 200 mg capsules because they may have been mislabeled as other prescription drugs.

    Product
    PREGABALIN, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00071101768.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Bumetanide Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Bumetanide 0.5 mg tablets because they may have been mislabeled as Erythromycin DR EC 250 mg.

    Product
    BUMETANIDE, Tablet, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093423201.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Mislabeled glyBURIDE Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling glyBURIDE tablets that may have been mislabeled as other prescription drugs. The error poses a risk of patients receiving incorrect medication.

    Product
    glyBURIDE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093834301.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Multivitamin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling specific lots of multivitamin chew tablets because they may have been mislabeled as other drugs.

    Product
    MULTIVITAMIN/MULTIMINERAL, CHEW Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536344308.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Valsartan Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Valsartan 80 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    VALSARTAN, Tablet, 80 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00078035834.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Phenobarbital Tablets Due to Potential Pregabalin Labeling Error

    Aidapak Services is recalling Phenobarbital tablets that may be mislabeled as Pregabalin capsules. The error poses a risk of patients receiving the wrong medication.

    Product
    PHENobarbital, Tablet, 64.8 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603516721.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Losartan Potassium Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Losartan Potassium 25 mg tablets because they may have been mislabeled as Phytonadione 5 mg.

    Product
    LOSARTAN POTASSIUM, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093736498.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Varenicline Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Varenicline 0.5 mg tablets because they may have been mislabeled as other prescription drugs. The recall covers specific lots distributed in four western states.

    Product
    VARENICLINE, Tablet, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00069046856.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Trihexyphenidyl Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Trihexyphenidyl HCL tablets because they may have been mislabeled as Perphenazine tablets.

    Product
    TRIHEXYPHENIDYL HCL, Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00591533501.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Niacin ER Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Niacin ER 500 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    NIACIN ER, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00074307490.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Thyroid Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 30 mg Thyroid tablets because they may have been mislabeled as other prescription drugs.

    Product
    THYROID, Tablet, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00456045801.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Aspirin Chew Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 81 mg aspirin chew tablets because they may have been mislabeled as other medications, including modafinil and omega-3 fatty acids.

    Product
    ASPIRIN, CHEW Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536329736.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Oxybutynin Chloride Tablets Due to Labeling Errors

    Aidapak Services, LLC is recalling Oxybutynin Chloride 5 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    OXYBUTYNIN CHLORIDE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603497521.
    Category
    Distribution
    4 states