Aidapak Recalls Pyridoxine HCL Tablets Due to Potential Labeling Errors
Aidapak Services, LLC is recalling 50 mg Pyridoxine HCL tablets because they may have been mislabeled as other medications. The affected products were distributed in four western states.
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 mixup. Per the rubric, minor labeling errors and voluntary precautionary recalls without reported injuries are rated as Moderate.
Plain-English summary
Aidapak Services, LLC is voluntarily recalling 695 tablets of Pyridoxine HCL, 50 mg, Over The Counter (NDC 00536440801). The recall is due to a labeling error where the product may have been mislabeled as Lactobacillus GG, Levothyroxine/Liothyronine, or Calcium/Cholecalciferol/Sodium.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The source text lists specific pedigree codes and expiration dates for the affected lots, including W003824 (EXP: 6/27/2014), AD30197_22 (EXP: 5/9/2014), and AD60428_10 (EXP: 5/22/2014).
Consumers should check their medication labels against the NDC and pedigree codes provided in the official recall notice. If the product matches the description, consumers should stop using it and contact their pharmacist or the recalling firm for instructions on return or disposal.
The recalled product
- Product
- PYRIDOXINE HCL, Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536440801.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-The-Counter
- Hazard
- Affected units
- 695
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 (8)
- PYRIDOXINE HCL
- Tablet
- 50 mg has the following codes: Pedigree: W003824
- EXP: 6/27/2014
- Pedigree: AD30197_22
- EXP: 5/9/2014
- Pedigree: AD60428_10
- EXP: 5/22/2014.
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.
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