Manufacturer
538 recalls in our database name Aidapak Services, LLC as the manufacturing or recalling firm.
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.
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.
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.
Aidapak Services, LLC is recalling 100-tablet bottles of Bisacodyl EC 5 mg tablets because they may be mislabeled as Cholecalciferol 400 units.
Aidapak Services is recalling Lactobacillus Acidophilus capsules because they may be mislabeled as Melatonin or Cranberry Extract products.
Aidapak Services, LLC is recalling Hydroxychloroquine Sulfate 200 mg tablets because they may be mislabeled as Guanfacine HCl 1 mg.
Aidapak Services is recalling 20 mg Fosinopril Sodium tablets that may be mislabeled as Tolterodine Tartrate ER capsules.
Aidapak Services, LLC is recalling Hydrocortisone 5 mg tablets that may be mislabeled as Orphenadrine Citrate ER or Calcium Acetate.
Aidapak Services is recalling Venlafaxine 25 mg tablets because they may be mislabeled as Omeprazole/Sodium Bicarbonate capsules.
Aidapak Services, LLC is recalling Quetiapine Fumarate 25 mg tablets because they may be mislabeled as Chlordiazepoxide HCl capsules.
Aidapak Services, LLC is recalling 150 mg Irbesartan tablets because they may be mislabeled as Atropine Sulfate/Diphenoxylate HCl or Cholecalciferol.
Aidapak Services, LLC is recalling 1 mg Glimepiride tablets because they may be mislabeled as Clomipramine HCl capsules.
Aidapak Services, LLC is recalling Glucosamine/Chondroitin capsules because they may be mislabeled as Fexofenadine HCL tablets.
Aidapak Services, LLC is recalling Atorvastatin Calcium 20 mg tablets because they may be mislabeled as GuaiFENesin ER 600 mg.
Aidapak Services, LLC is recalling aMILoride HCl 5 mg tablets because they may be mislabeled as Propranolol HCl 10 mg or Famotidine 20 mg.
Aidapak Services, LLC is recalling Pramipexole Di-HCl tablets because they may be mislabeled as Multivitamin/Multimineral or Perphenazine.
Aidapak Services, LLC is recalling Colestipol HCL Micronized Tablets because they may be mislabeled as rifAXIMin.
Aidapak Services, LLC is recalling Esterified Estrogens tablets because they may be mislabeled as Etodolac. The repacked drugs were distributed in four western states.
Aidapak Services is recalling RANOLAZINE ER 500 mg tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Lactobacillus tablets due to a label mixup that may cause them to be mislabeled as other medications.
Aidapak Services, LLC is recalling Riluzole 50 mg tablets due to a labeling error where they may be mislabeled as Trazodone HCl 150 mg.
Aidapak Services is recalling Galantamine HBr ER capsules because they may be mislabeled as Famotidine tablets.
Aidapak Services, LLC is recalling 3 mg Melatonin tablets because they may be mislabeled as other medications like Docusate Sodium or Pioglitazone.
Aidapak Services, LLC is recalling Vitamin B Complex Prolonged Release tablets because they may be mislabeled as guaiFENesin ER or tolterodine tartrate ER.
Aidapak Services, LLC is recalling 3 mg melatonin tablets distributed in four western states because they may be mislabeled as other supplements.
Aidapak Services, LLC is recalling Metaxalone 800 mg tablets because they may be mislabeled as Esterified Estrogens 0.625 mg.
Aidapak Services, LLC is recalling Calcium Citrate tablets that may be mislabeled as Triamterene/HCTZ. The repacked drugs were distributed in four western states.