Aidapak Recalls Pyridoxine HCL Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling 403 tablets of Pyridoxine HCL 50 mg because they may have been mislabeled as other medications. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a labeling error (label mixup) without reported illnesses or injuries, which aligns with the rubric for moderate severity involving minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling 403 tablets of Pyridoxine HCL, 50 mg, Over The Counter (NDC 00904052060). The recall was initiated because the tablets may have been mislabeled as other drugs, including Melatonin, Methocarbamol, Levothyroxine Sodium, or Riluzole. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
The affected product includes specific pedigree codes and expiration dates: AD22865_19 (EXP: 5/2/2014), AD46312_34 (EXP: 5/16/2014), AD22865_22 (EXP: 5/2/2014), and W003257 (EXP: 6/17/2014). Consumers should check their medication bottles for these specific codes and expiration dates to determine if they are affected.
Consumers who have purchased or possess these specific lots of Pyridoxine HCL tablets should stop using them and contact their healthcare provider or pharmacist for guidance. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- PYRIDOXINE HCL, Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052060.
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 403
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (9)
- PYRIDOXINE HCL
- Tablet
- 50 mg has the following codes: Pedigree: AD22865_19
- EXP: 5/2/2014
- Pedigree: AD46312_34
- EXP: 5/16/2014
- Pedigree: AD22865_22
- Pedigree: W003257
- EXP: 6/17/2014.
Distribution
Part of a larger recall action
This product is one of 265 recalled by Aidapak Services, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 265 products in this recall →Related recalls
Same manufacturer · Aidapak Services, LLC
See all →- ModerateAidapak Recalls Sennosides Tablets Due to Potential Labeling Errors
FDA (Drugs) · 2014-01-29
- ModerateLevothyroxine Sodium Tablets Recalled for Potential Labeling Mixup
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Mislabeled Pantoprazole Sodium DR Tablets
FDA (Drugs) · 2014-01-29
- ModerateAidapak Recalls Nifedipine ER Tablets Due to Potential Label Mixup
FDA (Drugs) · 2014-01-29
- ModerateSimvastatin Tablets Recalled for Potential Labeling Error
FDA (Drugs) · 2014-01-29
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02