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

251–265 of 265

  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Nefazodone 200 mg Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Nefazodone HCL 200 mg tablets because they may have been mislabeled as 150 mg tablets.

    Product
    NEFAZODONE HCL, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093102506.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Levothyroxine Sodium Tablets Due to Labeling Errors

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

    Product
    LEVOTHYROXINE SODIUM, Tablet, 88 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781518392.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Repaglinide Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Repaglinide 1 mg tablets because they may have been mislabeled as Valsartan, Guaifenesin, or Magnesium Chloride.

    Product
    REPAGLINIDE, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00169008281.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Prednisone Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling prednisone 20 mg tablets that may have been mislabeled as methylprednisolone 4 mg.

    Product
    predniSONE, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591544301.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Simvastatin Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Simvastatin 5 mg tablets that may be mislabeled as Losartan Potassium 25 mg.

    Product
    SIMVASTATIN, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093715298.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Exemestane Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Exemestane 25 mg tablets because they may be mislabeled as Omega-3 Fatty Acid capsules.

    Product
    EXEMESTANE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054008013.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Midodrine HCL Tablets Recalled for Potential Labeling Error

    Aidapak Services, LLC is recalling Midodrine HCL 2.5 mg tablets that may have been mislabeled as Pioglitazone HCL 15 mg.

    Product
    MIDODRINE HCL, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00185004001.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Fenofibrate Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling specific lots of Fenofibrate 54 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    FENOFIBRATE, Tablet, 54 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378710077.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Multivitamin Chew Tablets Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Multivitamin/Multimineral Chew Tablets due to a potential label mixup with Cholecalciferol capsules. The mislabeled products were distributed in four western states.

    Product
    MULTIVITAMIN/MULTIMINERAL W/IRON, CHEW Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536781601.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Raloxifene HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Raloxifene HCL tablets due to a potential label mixup with Isosorbide Mononitrate.

    Product
    RALOXIFENE HCL, Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002416530.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls CapsuleTOPRIL Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling CapsuleTOPRIL tablets because they may have been mislabeled as Calcitriol capsules. The error could lead to patients receiving the wrong medication.

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

    Mycophenolate Mofetil Capsules Recalled for Potential Label Mixup

    Aidapak Services is recalling Mycophenolate Mofetil capsules due to a potential label mixup with Calcium Acetate.

    Product
    MYCOPHENOLATE MOFETIL, Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00004025901.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Venlafaxine HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Venlafaxine HCL 100 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    VENLAFAXINE HCL, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093738301.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    Aidapak Recalls Calcitriol Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Calcitriol 0.25 mcg capsules because they may be mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    CALCITRIOL, Capsule, 0.25 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054000725.
    Category
    Distribution
    4 states