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

126–150 of 265

  • ModerateFDA (Drugs)··2014-01-29

    Fluvastatin Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Fluvastatin 20 mg capsules because they may have been mislabeled as a different medication.

    Product
    FLUVASTATIN, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378802077.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Ascorbic Acid Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Ascorbic Acid chew tablets because they may have been mislabeled as Phenol lozenges.

    Product
    ASCORBIC ACID, CHEW Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052660.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Vitamin B Complex Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Vitamin B Complex tablets because they may have been mislabeled as other drugs. The repacked products were distributed in four western states.

    Product
    VITAMIN B COMPLEX W/C, Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904026013.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Calcium Acetate Tablets Recalled for Potential Labeling Errors

    Aidapak Services is recalling Calcium Acetate tablets that may be mislabeled as Ascorbic Acid or Hyoscyamine Sulfate.

    Product
    CALCIUM ACETATE, Tablet, 667 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00574011302.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Repacked Progesterone Capsules Due to Potential Labeling Error

    Aidapak Services is recalling repacked progesterone capsules that may be mislabeled as levothyroxine sodium tablets. The error could lead to patients receiving the wrong medication.

    Product
    PROGESTERONE, Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00032170801.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    Venlafaxine HCL Tablets Recalled for Potential Labeling Errors

    Aidapak Services, LLC is recalling Venlafaxine HCL 25 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    VENLAFAXINE HCL, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093019901.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    FDA Recalls Calcium Acetate Capsules Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Calcium Acetate capsules because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    CALCIUM ACETATE, Capsule, 667 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00054008826.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Sotalol HCL Tablets Recalled for Potential Labeling Mixup

    Aidapak Services, LLC is recalling Sotalol HCL 160 mg tablets that may have been mislabeled as Disulfiram 250 mg.

    Product
    SOTALOL HCL, Tablet, 160 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093106201.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Bromocriptine Mesylate Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 2.5 mg Bromocriptine Mesylate tablets because they may have been mislabeled as Benazepril HCl or Thioridazine HCl.

    Product
    BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574010603.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Pyridoxine HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Pyridoxine HCL 25 mg tablets because they may have been mislabeled as Torsemide 10 mg.

    Product
    PYRIDOXINE HCL, Tablet, 25 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536440601.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Perphenazine Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling Perphenazine 16 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    PERPHENAZINE, Tablet, 16 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603506321.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Bromocriptine Mesylate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Bromocriptine Mesylate 2.5 mg tablets because they may have been mislabeled as Cyanocobalamin 1000 mcg.

    Product
    BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781532531.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Paricalcitol Capsules Due to Potential Labeling Errors

    Aidapak Services is recalling Paricalcitol capsules because they may have been mislabeled as Ascorbic Acid or Cholecalciferol.

    Product
    PARICALCITOL, Capsule, 1 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00074431730.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Mislabeled Quinidine Sulfate Tablets Distributed by Aidapak

    Aidapak Services, LLC is recalling Quinidine Sulfate 200 mg tablets that may have been mislabeled as Quinapril 40 mg. The error occurred during repacking in four western states.

    Product
    quiNIDine SULFATE, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591543801.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Thyroid Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 60 mg Thyroid tablets that may have been mislabeled as 30 mg tablets.

    Product
    THYROID, Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00456045901.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Ascorbic Acid Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 500 mg Ascorbic Acid tablets because they may have been mislabeled as Venlafaxine HCL 100 mg.

    Product
    ASCORBIC ACID, Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052372.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Tolterodine Tartrate ER Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Tolterodine Tartrate ER capsules because they may be mislabeled as Ranolazine ER or Ferrous Sulfate.

    Product
    TOLTERODINE TARTRATE ER, Capsule, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00009519001.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Verapamil Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Verapamil HCL tablets because they may have been mislabeled as Atorvastatin or Tacrolimus.

    Product
    VERAPAMIL HCL, Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591040401.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    Aidapak Recalls Loxapine Capsules Due to Potential Sertraline Labeling Error

    Aidapak Services, LLC is recalling Loxapine 5 mg capsules that may have been mislabeled as Sertraline HCL 50 mg tablets. The repacked drugs were distributed in four western states.

    Product
    LOXAPINE, Capsule, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591036901.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Thiothixene Capsules Recalled for Potential Labeling Error

    Aidapak Services is recalling Thiothixene 1 mg capsules because they may have been mislabeled as Omega-3 Fatty Acid 1000 mg capsules.

    Product
    THIOTHIXENE, Capsule, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378100101.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Cyanocobalamin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 923 tablets of Cyanocobalamin 1000 mcg because they may have been mislabeled as other medications.

    Product
    CYANOCOBALAMIN, Tablet, 1000 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536355601.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    Aidapak Recalls Metoprolol Tartrate Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 50 mg metoprolol tartrate tablets because they may have been mislabeled as other medications.

    Product
    METOPROLOL TARTRATE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093073301.
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-29

    FDA Recalls Levothyroxine Sodium Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Levothyroxine Sodium 88 mcg tablets because they may have been mislabeled as Guanfacine HCl 1 mg tablets.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 88 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00527134401.
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-29

    FDA Recalls Fenofibrate Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Fenofibrate 54 mg tablets that may have been mislabeled as Famciclovir 500 mg.

    Product
    FENOFIBRATE, Tablet, 54 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00115551110.
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-29

    FDA Recalls Mislabeled Acetaminophen, Butalbital, and Caffeine Tablets

    Aidapak Services, LLC is recalling Acetaminophen/Butalbital/Caffeine tablets that may have been mislabeled as Aspirin. The error could cause patients to take the wrong medication.

    Product
    ACETAMINOPHEN/ BUTALBITAL/ CAFFEINE, Tablet, 325 mg/50 mg/40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603254421.
    Category
    Distribution
    4 states