FDA Recalls Doxazosin Mesylate Tablets Due to Potential Labeling Error
Aidapak Services, LLC is recalling Doxazosin Mesylate 1 mg tablets that may be mislabeled as Pyridoxine HCl 100 mg.
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, which typically involves a labeling error that could lead to a temporary or medically reversible adverse health consequence. The rubric assigns a score of 2 to minor labeling errors and low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling Doxazosin Mesylate, Tablet, 1 mg, Over The Counter, NDC 00093812001. The recall is due to a labeling error where the product may have been mislabeled as Pyridoxine HCl, Tablet, 100 mg, NDC 00536440901.
The affected product is identified by Pedigree W003912 and an expiration date of 6/28/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the specific NDC and pedigree codes listed above. If the product matches the description, they should stop using it and contact their pharmacist or healthcare provider for guidance.
The recalled product
- Product
- DOXAZOSIN MESYLATE, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00093812001.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Tablets
- Hazard
- Affected units
- 100
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 (4)
- DOXAZOSIN MESYLATE
- Tablet
- 1 mg has the following codes: Pedigree: W003912
- EXP: 6/28/2014.
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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