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

251–273 of 273

  • HighFDA (Drugs)··2014-01-22

    Nicotine Polacrilex Lozenges Recalled for Potential Label Mixup

    Aidapak Services is recalling 1,582 Nicotine Polacrilex Lozenges because they may be mislabeled as other prescription drugs.

    Product
    NICOTINE POLACRILEX Lozenge, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 37205098769
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Mislabeled HydrALAZINE HCl Tablets

    Aidapak Services, LLC is recalling hydrALAZINE HCl 50 mg tablets that may be mislabeled as CapsuleTOPRIL 12.5 mg tablets.

    Product
    hydrALAZINE HCl Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111032801
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Chlorophyllin Copper Complex Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Chlorophyllin Copper Complex tablets that may be mislabeled as trazodone hydrochloride.

    Product
    CHLOROPHYLLIN COPPER COMPLEX, Tablet, 100 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 11868000901
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Paroxetine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Paroxetine HCl 10 mg tablets because they may be mislabeled as Pantoprazole Sodium DR 20 mg.

    Product
    PARoxetine HCl, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13107015430
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Doxepin HCL Capsules Recalled for Potential Label Mixup

    Aidapak Services is recalling Doxepin HCL capsules due to a labeling error where they may be mislabeled as Valsartan tablets.

    Product
    DOXEPIN HCL Capsule, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884022201
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Bisacodyl Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling 100-tablet bottles of Bisacodyl EC 5 mg tablets because they may be mislabeled as Cholecalciferol 400 units.

    Product
    BISACODYL EC, Tablet, 5 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904792760
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Lurasidone HCl Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Lurasidone HCl 120 mg tablets because they may be mislabeled as Duloxetine HCl DR 20 mg capsules.

    Product
    LURASIDONE HCL, Tablet, 120 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63402031230
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    FDA Recalls Pimozide Tablets Due to Potential Metoprolol Labeling Error

    Aidapak Services is recalling Pimozide 1 mg tablets that may be mislabeled as Metoprolol Tartrate 12.5 mg. The error poses a risk of incorrect medication administration.

    Product
    PIMOZIDE Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57844018701
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls GuaiFENesin ER Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling GuaiFENesin ER tablets because they may be mislabeled as Omega-3 acid ethyl esters capsules.

    Product
    guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000850
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Caffeine Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 200 mg caffeine tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    CAFFEINE Tablet, 200 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24385060173
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Metoprolol Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Metoprolol Tartrate 25 mg tablets because they may be mislabeled as Ascorbic Acid or Amlodipine Besylate.

    Product
    METOPROLOL TARTRATE Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050652
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Isosorbide Dinitrate Tablets Due to Labeling Error

    Aidapak Services is recalling Isosorbide Dinitrate ER tablets because they may be mislabeled as Cilostazol. Patients should check their medication labels.

    Product
    ISOSORBIDE DINITRATE ER Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664060088
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    FDA Recalls Glucosamine/Chondroitin Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Glucosamine/Chondroitin DS tablets because they may be mislabeled as Docusate Sodium capsules. The error could lead to patients taking the wrong medication.

    Product
    GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904559293
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Fluconazole Tablets Recalled Due to Potential Labeling Mixup

    Aidapak Services is recalling Fluconazole 100 mg tablets because they may be mislabeled as Prenatal Multivitamin/Multimineral tablets.

    Product
    FLUCONAZOLE, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462010230
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Phosphorus Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 250 mg Phosphorus tablets because they may be mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    PHOSPHORUS Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980010401
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Venlafaxine Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Venlafaxine 25 mg tablets because they may be mislabeled as Omeprazole/Sodium Bicarbonate capsules.

    Product
    VENLAFAXINE Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714031101
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Lactobacillus Tablets Recalled for Potential Labeling Errors

    Aidapak Services, LLC is recalling Lactobacillus tablets due to a label mixup that may cause them to be mislabeled as other medications.

    Product
    LACTOBACILLUS Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980012950
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Tizanidine Tablets Due to Potential Labeling Mixup

    Aidapak Services is recalling Tizanidine HCl tablets because they may be mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    tiZANidine HCl Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55111017915
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Etodolac Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Etodolac 400 mg tablets due to a potential label mixup with Pancrelipase DR capsules.

    Product
    ETODOLAC Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672401801
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Aspirin EC Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Aspirin EC DR tablets because they may be mislabeled as Melatonin or Docusate Sodium.

    Product
    ASPIRIN EC DR Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348098015
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Pyridoxine HCL Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Pyridoxine HCL 50 mg tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    PYRIDOXINE HCL Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 51645090901
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Omega-3 Fatty Acid Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Omega-3 Fatty Acid Capsules, 1000 mg, because they may be mislabeled as other medications. The affected products were distributed in Arizona, California, Oregon, and Washington.

    Product
    OMEGA-3 FATTY ACID Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 40985022921
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Multivitamin Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling specific lots of multivitamin capsules that may be mislabeled as caffeine or melatonin tablets.

    Product
    MULTIVITAMIN/ MULTIMINERAL/ LUTEIN Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24208063210
    Category
    Distribution
    4 states