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.

1–25 of 538

  • SevereFDA (Drugs)·D-893-2014·2014-01-29

    FDA Recalls Tizanidine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Tizanidine HCl 2 mg tablets that may have been mislabeled as Niacin TR 500 mg.

    Product
    tiZANidine HCl, Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378072219.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-940-2014·2014-01-29

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-847-2014·2014-01-29

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-959-2014·2014-01-29

    FDA Recalls Hyoscyamine Sulfate Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling 909 tablets of Hyoscyamine Sulfate SL 0.125 mg because they may have been mislabeled as other prescription drugs.

    Product
    HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574025001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-900-2014·2014-01-29

    Aidapak Recalls Atorvastatin Calcium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Atorvastatin Calcium 10 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    ATORVASTATIN CALCIUM, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378201577.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-827-2014·2014-01-29

    Aidapak Recalls Nortriptyline Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 10 mg Nortriptyline HCL capsules because they may have been mislabeled as 80 mg Valsartan tablets.

    Product
    NORTRIPTYLINE HCL, Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093081001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-839-2014·2014-01-29

    Aidapak Recalls Escitalopram Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 5 mg Escitalopram tablets because they may have been mislabeled as Sodium Chloride tablets.

    Product
    ESCITALOPRAM, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093585001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-856-2014·2014-01-29

    FDA Recalls Mislabeled Mexiletine HCL Capsules Distributed by Aidapak Services

    Aidapak Services, LLC is recalling 200 mg Mexiletine HCL capsules that may have been mislabeled as 10 mg Isosorbide Dinitrate tablets.

    Product
    MEXILETINE HCL, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093874001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-786-2014·2014-01-29

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-979-2014·2014-01-29

    Aidapak Recalls Minocycline Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Minocycline HCL capsules that may have been mislabeled as Progesterone. The repacked drugs were distributed in four western states.

    Product
    MINOCYCLINE HCL, Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591569550.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-895-2014·2014-01-29

    Aidapak Recalls Guanfacine HC Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling Guanfacine HC tablets because they may have been mislabeled as other prescription drugs. The repacked drugs were distributed in four western states.

    Product
    guanFACINE HC, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378116001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-923-2014·2014-01-29

    FDA Recalls Levothyroxine Sodium Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling Levothyroxine Sodium 175 mcg tablets because they may have been mislabeled as other medications.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 175 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00527135001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-779-2014·2014-01-29

    FDA Recalls Potentially Mislabeled Sirolimus Tablets Distributed by Aidapak Services

    Aidapak Services is recalling 1 mg Sirolimus tablets that may be mislabeled as Propranolol or Hydrocortisone. The repacked drugs were distributed in four western states.

    Product
    SIROLIMUS, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00008104105.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-859-2014·2014-01-29

    Terbutaline Sulfate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Terbutaline Sulfate 2.5 mg tablets because they may have been mislabeled as Sotalol HCl 80 mg.

    Product
    TERBUTALINE SULFATE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00115261101.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-989-2014·2014-01-29

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-887-2014·2014-01-29

    Aidapak Recalls Rosuvastatin Calcium Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling 5 mg rosuvastatin calcium tablets because they may have been mislabeled as ibuprofen or ascorbic acid.

    Product
    ROSUVASTATIN CALCIUM, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00310075590.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1022-2014·2014-01-29

    Aidapak Recalls Thiamine HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Thiamine HCL 100 mg tablets because they may have been mislabeled as other drugs, including simvastatin and buprenorphine.

    Product
    THIAMINE HCL, Tablet, 100 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904054460.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-981-2014·2014-01-29

    FDA Recalls Bismuth Subsalicylate Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Bismuth Subsalicylate chewable tablets that may have been mislabeled as Irbesartan. The error could lead to patients taking the wrong medication.

    Product
    BISMUTH SUBSALICYLATE, CHEW Tablet, 262 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00603023516.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1014-2014·2014-01-29

    FDA Recalls Chlorpromazine Tablets Due to Potential Labeling Error

    Aidapak Services is recalling chlorpromazine HCl tablets that may be mislabeled as acamprosate calcium. The error could lead to patients receiving the wrong medication.

    Product
    chlorproMAZINE HCl, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00832030200.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-977-2014·2014-01-29

    Minoxidil Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Minoxidil 2.5 mg tablets because they may have been mislabeled as methylprednisolone 4 mg.

    Product
    MINOXIDIL, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591564201.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-854-2014·2014-01-29

    Aidapak Recalls Mislabeled glyBURIDE Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling glyBURIDE tablets that may have been mislabeled as other prescription drugs. The error poses a risk of patients receiving incorrect medication.

    Product
    glyBURIDE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093834301.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-998-2014·2014-01-29

    FDA Recalls Perphenazine Tablets Due to Potential Label Mixup

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

    Product
    PERPHENAZINE, Tablet, 16 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781104901.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1019-2014·2014-01-29

    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
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1008-2014·2014-01-29

    Aidapak Recalls Mislabeled Methylprednisolone Tablets

    Aidapak Services, LLC is recalling methylprednisolone tablets that may have been mislabeled as levothyroxine, nabumetone, or cholecalciferol.

    Product
    methylPREDNISolone, Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781502201.
    Category
    Drug
    Distribution
    4 states