Aidapak Recalls Multivitamin Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling multivitamin tablets that may be mislabeled as lisinopril. The error could lead to patients taking the wrong medication.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe rating under the rubric. The hazard involves a potential mixup between a multivitamin and a prescription medication (lisinopril), which could result in significant health consequences if the wrong drug is taken.
Plain-English summary
Aidapak Services, LLC is recalling a specific lot of multivitamin/multimineral tablets due to a labeling error. The product, identified by NDC 00904549213 and pedigree AD23082_13, may be potentially mislabeled as lisinopril tablets, 2.5 mg (NDC 64679092701, pedigree AD25264_4).
The recall is being conducted because the multivitamin tablets may be confused with the prescription blood pressure medication lisinopril. This mixup poses a risk to patients who may inadvertently take the wrong medication. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the NDC 00904549213 and pedigree AD23082_13. If found, they should stop using the product and contact their pharmacist or healthcare provider for guidance on proper disposal or replacement.
The recalled product
- Product
- MULTIVITAMIN/MULTIMINERAL, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904549213
- Manufacturer
- Aidapak Services, LLC
- Affected units
- 520
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 (3)
- MULTIVITAMIN/MULTIMINERAL
- Tablet has the following code Pedigree: AD23082_13
- EXP: 11/1/2013.
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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