Fosinopril Sodium Tablets Recalled for Potential Labeling Error
Aidapak Services is recalling 10 mg Fosinopril Sodium tablets that may be mislabeled as Mercaptopurine 50 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 health consequence, fitting the Moderate severity criteria for minor labeling errors.
Plain-English summary
Aidapak Services, LLC is recalling specific lots of Fosinopril Sodium, Tablet, 10 mg (NDC 00185004109). The recall is due to a labeling error where the product may have been mislabeled as Mercaptopurine, Tablet, 50 mg (NDC 00054458111).
The affected product has the pedigree AD54549_7 and an expiration date of 5/20/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers and healthcare providers should check their inventory for this specific product and stop using it if the label is incorrect. They should contact their pharmacist or the recalling firm for instructions on how to return the product.
The recalled product
- Product
- FOSINOPRIL SODIUM, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00185004109.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 90
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)
- FOSINOPRIL SODIUM
- Tablet
- 10 mg has the following codes: Pedigree: AD54549_7
- EXP: 5/20/2014.
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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