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; NIACIN TR, Tablet, 500 mg may be potentially mislabeled as LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: W002968, EXP: 6/11/2014.

Labeling: Label Mixup; HYOSCYAMINE SULFATE ER Tablet, 0.375 mg may be potentially mislabeled as SERTRALINE HCL, Tablet, 50 mg, NDC 16714061204, Pedigree: W003575, EXP: 6/24/2014.

Labeling: Label Mixup; buPROPion HCl ER Tablet, 200 mg may be potentially mislabeled as AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W002726, EXP: 6/6/2014.

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 273

  • ModerateFDA (Drugs)··2014-01-22

    Carbamazepine ER Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling carbamazepine ER tablets that may be mislabeled as acarbose due to a label mixup.

    Product
    carBAMazepine ER Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672412401
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Aidapak Recalls GuaiFENesin ER Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling GuaiFENesin ER 600 mg tablets because they may be mislabeled as other prescription drugs.

    Product
    guaiFENesin ER, Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000815
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Zinc Sulfate Capsules Recalled for Potential Labeling Errors

    Aidapak Services is recalling Zinc Sulfate capsules that may be mislabeled as Calcium Acetate or Calcitrol due to a labeling mixup.

    Product
    ZINC SULFATE Capsule, 220 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258013101
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Melatonin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 1 mg Melatonin tablets that may be mislabeled as Omega-3 fatty acid capsules. The error involves a potential mix-up between two different products.

    Product
    MELATONIN, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 74312002832
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Aidapak Recalls Propranolol HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Propranolol HCL 10 mg tablets that may be mislabeled as Pioglitazone HCL 15 mg. The repacked drugs were distributed in four western states.

    Product
    PROPRANOLOL HCL, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714002104
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Omega-3 Fatty Acid Capsules Recalled for Potential Labeling Error

    Aidapak Services is recalling 1000 mg Omega-3 Fatty Acid capsules because they may be mislabeled as Nortriptyline HCL 50 mg.

    Product
    OMEGA-3 FATTY ACID, Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 05445800022
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Methylergonovine Maleate Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Methylergonovine Maleate tablets because they may be mislabeled as Isosorbide Mononitrate or Levothyroxine Sodium.

    Product
    METHYLERGONOVINE MALEATE Tablet, 0.2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386014028
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Lactobacillus Acidophilus Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Lactobacillus Acidophilus capsules because they may be mislabeled as Docusate Sodium. Consumers should stop using the product.

    Product
    LACTOBACILLUS ACIDOPHILUS Capsule, 500 Million CFU, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 43292055746
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Niacin TR Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Niacin TR tablets because they may be mislabeled as Solifenacin Succinate.

    Product
    NIACIN TR, Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 10939043533
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Warfarin Sodium Tablets Recalled Due to Potential Labeling Error

    Aidapak Services is recalling Warfarin Sodium 0.5 mg tablets that may be mislabeled as Sodium Chloride 1 mg tablets.

    Product
    WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 51672402701
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Rifaximin Tablets Recalled for Potential Mislabeling as Toprol

    Aidapak Services is recalling Rifaximin 200 mg tablets that may be mislabeled as Toprol 25 mg. The repacked drugs were distributed in four western states.

    Product
    rifAXIMin Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65649030103
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Melatonin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 3 mg melatonin tablets distributed in four western states because they may be mislabeled as other supplements.

    Product
    MELATONIN, Tablet, 3 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 08770140813
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Galantamine Capsules Due to Potential Labeling Error

    Aidapak Services is recalling Galantamine HBr ER capsules because they may be mislabeled as Famotidine tablets.

    Product
    GALANTAMINE HBr ER, Capsule, 8 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 10147089103
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    FDA Recalls Esterified Estrogens Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Esterified Estrogens tablets because they may be mislabeled as Etodolac. The repacked drugs were distributed in four western states.

    Product
    ESTERIFIED ESTROGENS Tablet, 0.625 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 61570007301
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Colestipol Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Colestipol HCL Micronized Tablets because they may be mislabeled as rifAXIMin.

    Product
    COLESTIPOL HCL MICRONIZED Tablet, 1 g, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762045001
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    FDA Recalls FIDAXOMICIN Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling FIDAXOMICIN 200 mg tablets that may be mislabeled as BENAZEPRIL HCL 40 mg. The error affects repacked drugs distributed in four western states.

    Product
    FIDAXOMICIN Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 52015008001
    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 20 mg tablets because they may be mislabeled as GuaiFENesin ER 600 mg.

    Product
    ATORVASTATIN CALCIUM Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505257909
    Category
    Distribution
    4 states
  • SevereFDA (Drugs)··2014-01-22

    Aidapak Recalls Nifedipine Capsules Due to Potential Labeling Error

    Aidapak Services is recalling Nifedipine 10 mg capsules because they may be mislabeled as Nitrofurantoin 100 mg. The repacked drugs were distributed in four western states.

    Product
    NIFEdipine Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762100401
    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
  • SevereFDA (Drugs)··2014-01-22

    Finasteride Tablets Recalled for Potential Mislabeling as Other Medications

    Aidapak Services is recalling Finasteride 5 mg tablets that may be mislabeled as Digoxin or Phytonadione. The error poses a risk of incorrect medication administration.

    Product
    FINASTERIDE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714052201
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Quetiapine Fumarate Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Quetiapine Fumarate 25 mg tablets because they may be mislabeled as Chlordiazepoxide HCl capsules.

    Product
    QUEtiapine FUMARATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65862048901
    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

    Aidapak Recalls Hydrocortisone Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Hydrocortisone 5 mg tablets that may be mislabeled as Orphenadrine Citrate ER or Calcium Acetate.

    Product
    HYDROCORTISONE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64720033105
    Category
    Distribution
    4 states
  • HighFDA (Drugs)··2014-01-22

    Leflunomide Tablets Recalled Due to Potential Labeling Mixup

    Aidapak Services is recalling Leflunomide 10 mg tablets because they may be mislabeled as Doxycycline or Sevelamer Carbonate.

    Product
    LEFLUNOMIDE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155004303
    Category
    Distribution
    4 states
  • ModerateFDA (Drugs)··2014-01-22

    Aidapak Recalls Multivitamin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling multivitamin tablets that may be mislabeled as quetiapine or docusate sodium. The recall covers specific lots distributed in four western states.

    Product
    MULTIVITAMIN/MULTIMINERAL Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 37205018581
    Category
    Distribution
    4 states