Aidapak Recalls Irbesartan Tablets Due to Potential Labeling Error
Aidapak Services is recalling 150 mg Irbesartan tablets because they may have been mislabeled as Benazepril HCl 40 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 and involves a labeling error (mislabeling) without reported illnesses or injuries, which aligns with the 'Moderate' severity criteria for minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling 30-tablet bottles of Irbesartan 150 mg tablets (NDC 00093746556) due to a labeling error. The source text indicates that the Irbesartan tablets may have been mislabeled as Benazepril HCl 40 mg tablets (NDC 65162075410).
The recalled Irbesartan tablets have the pedigree code AD42592_7 and an expiration date of 5/14/2014. The potentially mislabeled Benazepril HCl tablets have the pedigree code AD32757_7 and an expiration date of 5/13/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their medication for the specific NDC and pedigree codes listed above. If the medication matches the recalled description, they should stop using it and contact their pharmacist or healthcare provider for guidance.
The recalled product
- Product
- IRBESARTAN, Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093746556.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 30
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)
- IRBESARTAN
- Tablet
- 150 mg has the following codes: Pedigree: AD42592_7
- EXP: 5/14/2014.
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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