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Aidapak Services, LLC

Aidapak Services, LLC Recalls

All product recalls associated with Aidapak Services, LLC.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

34

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 15661–15680 of 21320 recalls

Guanfacine HCl Tablet (Aidapak Services) – Incorrect Label (2013)

Labeling: Label Mixup: guanFACINE HCl, Tablet, 1 mg may have potentially been mislabeled as one of the following drugs: buPROPion HCl ER, Tablet, 200 mg, NDC 47335073886, Pedigree: W002727, EXP: 6/6/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD39588_7, EXP: 5/13/2014; OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,100 mg, NDC 11523726503, Pedigree: W003873, EXP: 6/2

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Levothyroxine Sodium Tablet (Aidapak) – label mixup (2013)

Labeling: Label Mixup: LEVOTHYROXINE SODIUM, Tablet, 12.5 mcg (1/2 of 25 mcg) may have potentially been mislabeled as one of the following drugs: CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD30180_1, EXP: 5/8/2014; carBAMazepine ER, Capsule, 200 mg, NDC 66993040832, Pedigree: AD32764_14, EXP: 5/14/2014; CHLORTHALIDONE, Tablet, 12.5 mg (1/2 of 25 mg), NDC 00378022201, Pedigree:

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

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Olanzapine Tablet (Aidapak) – label mixup (2013)

Labeling:Label Mixup; OLANZapine, Tablet, 7.5 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 175 mcg, NDC 00527135001, Pedigree: AD46265_37, EXP: 5/15/2014; LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00781518392, Pedigree: AD60272_73, EXP: 5/22/2014; MIRTAZAPINE, Tablet, 7.5 mg, NDC 59762141503, Pedigree: AD73525_55, EXP: 5/30/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Mycophenolate Mofetil Capsule (Aidapak) – label mixup (2013)

Labeling: Label Mixup: MYCOPHENOLATE MOFETIL, Capsule, 250 mg may have potentially been mislabeled as the following drug: PRAMIPEXOLE DI-HCL, Tablet, 0.25 mg, NDC 16714058501, Pedigree: W003761, EXP: 6/26/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Minocycline HCL Capsule (Aidapak Services) – Incorrect Label (2013)

Labeling: Label Mixup: MINOCYCLINE HCL, Capsule, 50 mg may have potentially been mislabeled as the following drug: MINOXIDIL, Tablet, 2.5 mg, NDC 00591564201, Pedigree: AD52778_49, EXP: 5/20/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Pancrelipase DR Capsule (Aidapak Services) – Label Mix-up (2013)

Labeling: Label Mixup: PANCRELIPASE DR, Capsule, 12000 /38000 /60000 USP units may be potentially mislabeled as the following drug: ASPIRIN/ER DIPYRIDAMOLE, Capsule, 25 mg/200 mg, NDC 00597000160, Pedigree: AD70639_4, EXP: 7/28/2013.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Fosinopril Sodium Tablet (Aidapak) – label mixup (2013)

Labeling:Label Mixup; FOSINOPRIL SODIUM, Tablet, 20 mg may be potentially mislabeled as TOLTERODINE TARTRATE ER, Capsule, 2 mg, NDC 00009519001, Pedigree: AD65478_1, EXP: 5/29/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Diltiazem HCL ER Capsule (Aidapak Services) – Mislabeled Drug (2013)

Labeling: Label Mixup; DILTIAZEM HCL ER Capsule, 240 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 37205098769, Pedigree: AD52433_4, EXP: 5/17/2014; PARoxetine HCl, Tablet, 10 mg, NDC 13107015430, Pedigree: AD52778_67, EXP: 5/20/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Levothyroxine Sodium Tablet (Aidapak Services) – Label Swap (2013)

Labeling: Label Mixup: LEVOTHYROXINE SODIUM, Tablet, 175 mcg may have potentially been mislabeled as the following drug: CINACALCET HCL, Tablet, 60 mg, NDC 55513007430, Pedigree: W003742, EXP: 6/26/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Nefazodone HCL Tablet (Aidapak Services) – Label Error (2013)

Labeling: Label Mixup: NEFAZODONE HCL, Tablet, 200 mg may have potentially been mislabeled as the following drug: NEFAZODONE HCL, Tablet, 150 mg, NDC 00093711306, Pedigree: AD46414_41, EXP: 5/16/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Omega-3 Fatty Acid Capsule (Aidapak) – label mixup (2013)

Labeling: Label Mixup; OMEGA-3 FATTY ACID, Capsule, 1000 mg may be potentially mis-labeled as DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: AD33897_16, EXP: 5/9/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD33897_19, EXP: 5/9/2014; PSEUDOEPHEDRINE HCL, Tablet, 60 mg, NDC 00904512559, Pedigree: W002856, EXP: 6/7/2014; DOCUSATE SODIUM, Capsule, 50 mg, N

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Thioridazine HCL Tablet (Aidapak Services) – Mislabeled Medication (2013)

Labeling: Label Mixup: THIORIDAZINE HCL, Tablet, 50 mg may have potentially been mislabeled as the following drug: guanFACINE HCl, Tablet, 1 mg, NDC 00591044401, Pedigree: AD73525_13, EXP: 4/30/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Colchicine Tablet (Aidapak Services) – Incorrect Label (2013)

Labeling: Label Mixup; COLCHICINE Tablet, 0.6 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 2000 units, NDC 00904615760, Pedigree: AD46312_37, EXP: 5/16/2014; PSEUDOEPHEDRINE HCL, Tablet, 30 mg, NDC 00904505360, Pedigree: AD52993_37, EXP: 5/20/2014; SENNOSIDES, Tablet, 8.6 mg, NDC 00182109301, Pedigree: AD62992_14, EXP: 5/23/2014; CHOLECALCIFEROL, Tablet, 1000 units, NDC 00904

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Glimepiride Tablet (Aidapak) – label mixup (2013)

Labeling:Label Mixup; GLIMEPIRIDE, Tablet, 1 mg may be potentially mislabeled as clomiPRAMINE HCl, Capsule, 50 mg, NDC 51672401205, Pedigree: AD73525_4, EXP: 5/30/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Torsemide Tablet (Aidapak) – label mixup (2013)

Labeling: Label Mixup; TORSEMIDE Tablet, 10 mg may be potentially mislabeled as MEXILETINE HCL, Capsule, 200 mg, NDC 00093874001, Pedigree: AD25264_7, EXP: 5/3/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Carvedilol Phosphate ER Capsule (Aidapak) – Label Mixup (2013)

Labeling: Label Mixup: CARVEDILOL PHOSPHATE ER, Capsule, 20 mg may be potentially mislabeled as the following drug: BUMETANIDE, Tablet, 1 mg, NDC 00093423301, Pedigree: W003224, EXP: 6/17/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Amiloride HCl Tablet (Aidapak) – Label Mixup (2013)

Labeling: Label Mixup; aMILoride HCl Tablet, 5 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree: AD60272_37, EXP: 5/22/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003764, EXP: 6/26/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Cholecalciferol Capsule (Aidapak) – Label Mixup (2013)

Labeling: Label Mixup: CHOLECALCIFEROL, Capsule, 2000 units may have potentially been mislabeled as one of the following drugs: DOXYCYCLINE HYCLATE, Tablet, 100 mg, NDC 53489012002, Pedigree: AD30993_8, EXP: 5/9/2014; VITAMIN B COMPLEX PROLONGED RELEASE, Tablet, 50 mg, NDC 40985022251, Pedigree: AD60211_20, EXP: 5/21/2014; lamoTRIgine, Tablet, 50 mg (1/2 of 100 mg), NDC 13668004701, Pedigree: A

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Modafinil Tablet (Aidapak) – Label Mixup (2013)

Labeling:Label Mixup; MODAFINIL Tablet, 50 mg (1/2 of 100 mg Tablet) may be potentially mislabeled as SACCHAROMYCES BOULARDII LYO, Capsule, 250 mg, NDC 00414200007, Pedigree: AD21859_1, EXP: 10/31/2013.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC

Acetaminophen/Aspirin/Caffeine Tablet (Aidapak) – Label Mixup (2013)

Labeling: Label Mixup; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg may be potentially mislabeled as NAPROXEN, Tablet, 500 mg, NDC 53746019001, Pedigree: AD68025_8, EXP: 5/28/2014.

Class IIModerate

FDAJul 2, 2013AZ, CA, IN +2 more• Aidapak Services, LLC