Aidapak Recalls Benazepril HCL Tablets Due to Potential Labeling Errors
Aidapak Services, LLC is recalling 799 Benazepril HCL tablets because they may be mislabeled as other medications.
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, which fits the rubric criterion for minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling 799 Benazepril HCL tablets, 40 mg, NDC 65162075410. The recall is due to a labeling mixup where the product may be potentially mislabeled as other drugs, including Nefazodone HCL, GuaiFENesin ER, Calcium Acetate, and Acetaminophen/Aspirin/Caffeine.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. Specific pedigree codes and expiration dates for the affected Benazepril HCL tablets are AD49423_1 (EXP: 5/16/2014), W003918 (EXP: 6/28/2014), AD32757_7 (EXP: 5/13/2014), and AD68010_1 (EXP: 5/28/2014).
Consumers should check their medication for these specific codes and expiration dates. If the product matches the description, they should stop using it and contact their pharmacist or healthcare provider for guidance.
The recalled product
- Product
- BENAZEPRIL HCL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075410
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Tablets
- Hazard
- Affected units
- 799
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)
- BENAZEPRIL HCL Tablet
- 40 mg has the following codes Pedigree: AD49423_1
- EXP: 5/16/2014
- Pedigree: W003918
- EXP: 6/28/2014
- Pedigree: AD32757_7
- EXP: 5/13/2014
- Pedigree: AD68010_1
- EXP: 5/28/2014.
Distribution
Part of a larger recall action
This product is one of 273 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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