Lisinopril Tablets Recalled for Potential Labeling Errors
Aidapak Services is recalling Lisinopril 2.5 mg tablets because they may be mislabeled as Ranolazine ER or Docusate Sodium.
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 fall under the Moderate severity category.
Plain-English summary
Aidapak Services, LLC is recalling specific lots of Lisinopril Tablet, 2.5 mg, Rx only, NDC 64679092701. The recall is due to a labeling error where the product may be mislabeled as Ranolazine ER, Tablet, 500 mg, or Docusate Sodium, Capsule, 250 mg.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The specific codes for the recalled Lisinopril tablets are Pedigree AD25264_4 with an expiration date of 5/3/2014, and Pedigree W003365 with an expiration date of 6/19/2014.
Consumers and healthcare providers should check their inventory for these specific NDCs and pedigree codes. If the product is found, it should be returned to the distributor or disposed of according to local regulations. Patients should consult their healthcare provider if they have questions about their medication.
The recalled product
- Product
- LISINOPRIL Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679092701
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 300
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 (5)
- LISINOPRIL Tablet
- 2.5 mg has the following codes Pedigree: AD25264_4
- EXP: 5/3/2014
- Pedigree: W003365
- EXP: 6/19/2014.
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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