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

76–100 of 265

  • ModerateFDA (Drugs)··2014-01-29

    Repaglinide Tablets Recalled Due to Potential Labeling Mixup

    Aidapak Services is recalling Repaglinide 2 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    REPAGLINIDE, Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00169008481.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Pancrelipase DR Capsules Due to Potential Label Mixup

    Aidapak Services is recalling Pancrelipase DR capsules because they may be mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    PANCRELIPASE DR, Capsule, 12000 /38000 /60000 USP units, Rx only, Distributed by: AidaPak Service, LLC, NDC 00032121201.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Aspirin EC Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Aspirin EC tablets because they may have been mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    ASPIRIN EC, Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904201360.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Glyburide Tablets Due to Potential Label Mixup

    Aidapak Services is recalling glyBURIDE MICRONIZED tablets because they may have been mislabeled as digoxin. The error could lead to patients receiving the wrong medication.

    Product
    glyBURIDE MICRONIZED, Tablet, 3 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093803501.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Aspirin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 325 mg aspirin tablets because they may have been mislabeled as other prescription medications.

    Product
    ASPIRIN, Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536330501.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    FDA Recalls Famciclovir Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Famciclovir 500 mg tablets because they may have been mislabeled as Tolterodine or Thiamine.

    Product
    FAMCICLOVIR, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093811956.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Acarbose Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Acarbose 25 mg tablets because they may be mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    ACARBOSE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054014025.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Niacin Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Niacin 500 mg tablets because they may have been mislabeled as Naproxen or Docusate Sodium.

    Product
    NIACIN, Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904227260.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Ascorbic Acid Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling 500 mg Ascorbic Acid tablets that may have been mislabeled as Oxcarbazepine 150 mg.

    Product
    ASCORBIC ACID, Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052380.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Cyclobenzaprine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 5 mg cyclobenzaprine tablets because they may have been mislabeled as ascorbic acid or atenolol.

    Product
    CYCLOBENZAPRINE HCL, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591325601.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Selenium Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling 50 mcg selenium tablets that may be mislabeled as guaifenesin ER 600 mg.

    Product
    SELENIUM, Tablet, 50 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904316260.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Atorvastatin Calcium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Atorvastatin Calcium 10 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    ATORVASTATIN CALCIUM, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378201577.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Potassium Acid Phosphate Tablets Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Potassium Acid Phosphate tablets due to a potential label mixup with prednisone. The repacked drugs were distributed in four western states.

    Product
    POTASSIUM ACID PHOSPHATE, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00486111101.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Atorvastatin Calcium Tablets Due to Potential Label Mixup

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

    Product
    ATORVASTATIN CALCIUM, Tablet, 80 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378212277.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    Aidapak Recalls Aspirin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 81 mg Aspirin DR EC tablets because they may have been mislabeled as Sotalol HCl or Folic Acid.

    Product
    ASPIRIN DR EC, Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00182106105.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Hydrocortisone Tablets Due to Potential Labeling Errors

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

    Product
    HYDROCORTISONE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603389919.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Metoprolol Tartrate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Metoprolol Tartrate 25 mg tablets because they may have been mislabeled as Docusate Sodium 250 mg capsules.

    Product
    METOPROLOL TARTRATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378001801.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Saccharomyces Boulardii Capsules Recalled for Potential Label Mixup

    Aidapak Services is recalling Saccharomyces Boulardii capsules because they may have been mislabeled as other prescription drugs.

    Product
    SACCHAROMYCES BOULARDII LYO, Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00414200007.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Atomoxetine Capsules Due to Potential Label Mixup

    Aidapak Services is recalling Atomoxetine HCL capsules because they may be mislabeled as other psychiatric medications.

    Product
    ATOMOXETINE HCL, Capsule, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002322930.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Chlordiazepoxide Capsules Due to Potential Labeling Errors

    Aidapak Services is recalling 1,101 chlordiazepoxide capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.

    Product
    chlordiazePOXIDE HCl, Capsule, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00555015902.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Perphenazine Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Perphenazine 8 mg tablets that may have been mislabeled as Nifedipine 10 mg capsules.

    Product
    PERPHENAZINE, Tablet, 8 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00630506221.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Flecainide Acetate Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling Flecaainide Acetate tablets because they may be mislabeled as Colestipol HCL Micronized.

    Product
    FLECAINIDE ACETATE, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054001125.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Mislabeled Cyanocobalamin Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling 500 mcg Cyanocobalamin tablets that were mislabeled as Sevelamer Carbonate or other drugs. The recall covers products distributed in Arizona, California, Oregon, and Washington.

    Product
    CYANOCOBALAMIN, Tablet, 500 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536355101.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Dronedarone HCL Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Dronedarone HCL 400 mg tablets because they may be mislabeled as Methylergonovine Maleate 0.2 mg.

    Product
    DRONEDARONE HCL, Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00024414260.
    Category
    Distribution
    4 states