The Recall Desk

Manufacturer

Aidapak Services, LLC

538 recalls in our database name Aidapak Services, LLC as the manufacturing or recalling firm.

What the numbers show

Total
538
Critical
0
Severe
127
Most recent
2014-01-29

Of the 538 recalls from Aidapak Services, LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 127 (24%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

276–300 of 538

  • SevereFDA (Drugs)·D-689-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-484-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-615-2014·2014-01-22

    Lanthanum Carbonate Chew Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Lanthanum Carbonate Chew Tablets due to a potential label mixup with other medications. The repacked drugs were distributed in four western states.

    Product
    LANTHANUM CARBONATE Chew Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 54092025290
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-714-2014·2014-01-22

    Colesevelam HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Colesevelam HCL tablets that may be mislabeled as lamoTRIgine due to a labeling error.

    Product
    COLESEVELAM HCL Tablet, 625 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65597070118
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-697-2014·2014-01-22

    Aidapak Recalls Lubiprostone Capsules Due to Potential Labeling Errors

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

    Product
    LUBIPROSTONE Capsule, 24 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764024060
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-526-2014·2014-01-22

    FDA Recalls Mislabeled HydrALAZINE Tablets Due to Label Mixup

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

    Product
    hydrALAZINE HCl Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155000401
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-704-2014·2014-01-22

    Sodium Bicarbonate Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling 1,013 sodium bicarbonate tablets that may be mislabeled as nicotine polacrilex lozenges.

    Product
    SODIUM BICARBONATE Tablet, 650 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980018210
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-575-2014·2014-01-22

    FDA Recalls Mislabeled Quetiapine Fumarate Tablets Distributed by Aidapak

    Aidapak Services is recalling Quetiapine Fumarate tablets that may be mislabeled as Simvastatin. The FDA classifies this as a Class II recall.

    Product
    QUETIAPINE FUMARATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 47335090288
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-478-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-682-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-514-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-608-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-644-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-519-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-721-2014·2014-01-22

    Aidapak Recalls Docusate Sodium Capsules Due to Labeling Mixup

    Aidapak Services, LLC is recalling Docusate Sodium capsules because they may be mislabeled as other medications. The affected products were distributed in four western states.

    Product
    DOCUSATE SODIUM, Capsule, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 67618010060
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-597-2014·2014-01-22

    FDA Recalls TACROLIMUS Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling TACROLIMUS Capsules, 1 mg, because they may be mislabeled as LEVOTHYROXINE SODIUM Tablets, 125 mcg.

    Product
    TACROLIMUS Capsule, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50742020801
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-620-2014·2014-01-22

    FDA Recalls Tizanidine Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Tizanidine HCl tablets that may be mislabeled as Pyridoxine HCl. The error could lead to patients taking the wrong medication.

    Product
    tiZANidine HCl Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 55111017915
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-473-2014·2014-01-22

    FDA Recalls Calcium Citrate Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling calcium citrate tablets that may be mislabeled as trimethobenzamide HCL capsules.

    Product
    CALCIUM CITRATE, Tablet, 950 mg (200 MG ELEMENTAL Ca), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-474-2014·2014-01-22

    Calcium Citrate Tablets Recalled for Potential Lithium Carbonate Labeling Error

    Aidapak Services is recalling Calcium Citrate tablets that may be mislabeled as Lithium Carbonate ER. The error could lead to incorrect medication administration.

    Product
    CALCIUM CITRATE, Tablet, 950 mg (200 mg Elemental Calcium), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-641-2014·2014-01-22

    FDA Recalls Mislabeled Darunavir Tablets Distributed by Aidapak Services

    Aidapak Services is recalling Darunavir tablets that may be mislabeled as Hydrocodone/Acetaminophen. The error could lead to incorrect medication administration.

    Product
    DARUNAVIR Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59676056630
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-720-2014·2014-01-22

    Aidapak Recalls Selegiline HCL Capsules Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Selegiline HCL 5 mg capsules because they may be mislabeled as Itraconazole 100 mg. The repacked drugs were distributed in four western states.

    Product
    SELEGILINE HCL, Capsule, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67253070006
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-596-2014·2014-01-22

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-673-2014·2014-01-22

    Aidapak Recalls OXcarbazepine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling OXcarbazepine 150 mg tablets because they may be mislabeled as traZODone HCl 50 mg.

    Product
    OXcarbazepine Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018388
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-602-2014·2014-01-22

    Warfarin Sodium Tablets Recalled Due to Potential Label Mixup

    Aidapak Services is recalling Warfarin Sodium 0.5 mg tablets because they 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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-582-2014·2014-01-22

    Aspirin Tablets Recalled for Potential Mislabeling as Cholecalciferol

    Aidapak Services is recalling Aspirin tablets that may be mislabeled as Cholecalciferol. The FDA classifies this as a Class II recall.

    Product
    ASPIRIN Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348000123
    Category
    Drug
    Distribution
    4 states