The Recall Desk

FDA (Drugs) recall action 65707

Aidapak Services, LLC recalled 273 products on 2014-01-22

The FDA (Drugs) publishes a recall like this one as 273 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 273 pages.

Products
273
Announced
2014-01-22
Critical
0
Units
157,306

Why these products were recalled

Labeling:Label Mixup; sulfaSALAzine Tablet, 500 mg may be potentially mislabeled as HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, NDC 00574025001, Pedigree: AD46265_7, EXP: 5/15/2014.

Labeling:Label Mixup; CRANBERRY Tablet, 450 mg may be potentially mislabeled as METOPROLOL SUCCINATE ER, Tablet, 200 mg, NDC 62037083301, Pedigree: AD73652_13, EXP: 5/30/2014.

Labeling: Label Mixup; CHOLECALCIFEROL, Tablet, 2000 units may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00904052060, Pedigree: AD46312_34, EXP: 5/16/2014; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 13811051410, Pedigree: AD65314_1, EXP: 5/24/2014; RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: W003538, EXP: 6/21/2014; LEVOTHYROXINE SODIUM, Tablet, 175

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

126–150 of 273

  • ModerateFDA (Drugs)··2014-01-22

    Magnesium Gluconate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Magnesium Gluconate tablets that may be mislabeled as Fluvastatin capsules due to a label mixup.

    Product
    MAGNESIUM GLUCONATE Tablet, 500 mg (27 mg Elem Mg), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 35046000322
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Promethazine HCL Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Promethazine HCL tablets that may be mislabeled as Cholecalciferol due to a labeling mixup.

    Product
    PROMETHAZINE HCL, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162052110
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Aidapak Recalls Mislabeled Pantoprazole Sodium Tablets

    Aidapak Services, LLC is recalling 20 mg Pantoprazole Sodium tablets that may be mislabeled as Fosinopril Sodium. The error involves a label mixup on repacked drugs.

    Product
    PANTOPRAZOLE SODIUM DR Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679043304
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Flecaïnide Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Flecaïnide Acetate tablets that may be mislabeled as Vitamin B Complex with C due to a labeling error.

    Product
    FLECAINIDE ACETATE Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162064110
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Mislabeled Melatonin Tablets Distributed by Aidapak Services

    Aidapak Services is recalling 1 mg melatonin tablets that may be mislabeled as cranberry extract or glycopyrrolate. The FDA classifies this as a Class II recall.

    Product
    MELATONIN Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 35046000391
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Aidapak Recalls Guanfacine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling guanfacine HCl tablets because they may be mislabeled as other prescription medications.

    Product
    guanFACINE HCl Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162071310
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    FDA Recalls Potentially Mislabeled Losartan Potassium Tablets

    Aidapak Services is recalling Losartan Potassium tablets that may be mislabeled as Disopyramide Phosphate. The error involves a label mixup on repacked drugs.

    Product
    LOSARTAN POTASSIUM, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13668011390
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Rivaroxaban Tablets Recalled for Potential Venlafaxine Labeling Error

    Aidapak Services is recalling Rivaroxaban 20 mg tablets that may be mislabeled as Venlafaxine HCL 100 mg due to a label mixup.

    Product
    RIVAROXABAN Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50458057930
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Fluoxetine Capsules Recalled Due to Potential Labeling Error

    Aidapak Services is recalling Fluoxetine HCl capsules because they may be mislabeled as Pancrelipase DR.

    Product
    FLUoxetine HCl Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714035103
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    FDA Recalls Fexofenadine Tablets Due to Potential Labeling Mixup

    Aidapak Services is recalling Fexofenadine HCl tablets that may be mislabeled as Pyridoxine, Niacin, or Cranberry Extract.

    Product
    FEXOFENADINE HCl Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 45802042578
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Atorvastatin Calcium Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Atorvastatin Calcium 80 mg tablets because they may be mislabeled as Lactobacillus GG capsules.

    Product
    ATORVASTATIN CALCIUM, Tablet, 80 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505267109
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Ascorbic Acid Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling 500 mg Ascorbic Acid tablets that may be mislabeled as Febuxostat 40 mg. The error could lead to incorrect medication administration.

    Product
    ASCORBIC ACID Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258014101
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Quetiapine Fumarate Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling 1,300 Quetiapine Fumarate 100 mg tablets because they may be mislabeled as other medications.

    Product
    QUEtiapine FUMARATE Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505313301
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Cinacalcet HCL Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Cinacalcet HCL 60 mg tablets because they may be mislabeled as Ranolazine ER 500 mg.

    Product
    CINACALCET HCL Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55513007430
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Magnesium Chloride Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Magnesium Chloride tablets that may be mislabeled as Selegiline HCL or Phosphorus due to a label mixup.

    Product
    MAGNESIUM CHLORIDE DR, Tablet, 64 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904791152
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Diltiazem HCL ER Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Diltiazem HCL ER Capsules, 240 mg, because they may be mislabeled as Nicotine Polacrilex or Paroxetine HCl.

    Product
    DILTIAZEM HCL ER Capsule, 240 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884083109
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Ferrous Sulfate Tablets Due to Potential Label Mixup

    Aidapak Services is recalling ferrous sulfate tablets that may be mislabeled as ramipril capsules. The error involves a label mixup on repacked drugs.

    Product
    FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904759160
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Folic Acid Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling 1 mg Folic Acid tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    FOLIC ACID, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162036110
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Glucosamine/Chondroitin Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Glucosamine/Chondroitin capsules because they may be mislabeled as Fexofenadine HCL tablets.

    Product
    GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54458010022
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Multivitamin Chew Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Multivitamin/Multimineral Chew Tablets because they may be mislabeled as Levothyroxine Sodium or Lactobacillus Acidophilus.

    Product
    MULTIVITAMIN/MULTIMINERAL Chew Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 58914001460
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls OXcarbazepine Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling OXcarbazepine 600 mg tablets that may be mislabeled as Lactase Enzyme 3000 units. The error could lead to patients receiving the wrong medication.

    Product
    OXcarbazepine Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018588
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Zinc Sulfate Capsules Recalled for Potential Mislabeling as Sertraline

    Aidapak Services is recalling Zinc Sulfate capsules that may be mislabeled as Sertraline HCL tablets. The error could lead to patients taking the wrong medication.

    Product
    ZINC SULFATE, Capsule, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904533260
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Aidapak Recalls Prenatal Multivitamin Tablets Due to Labeling Errors

    Aidapak Services, LLC is recalling prenatal multivitamin tablets that may be mislabeled as other medications like riluzole or aspirin.

    Product
    PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904531360
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Cilostazol Tablets Recalled for Potential Labeling Mixup with Dutasteride

    Aidapak Services is recalling Cilostazol 100 mg tablets due to a labeling mixup where they may be mislabeled as Dutasteride 0.5 mg capsules.

    Product
    CILOSTAZOL Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505252201
    Category
    Distribution
    4 states