Nifedipine Capsules Recalled for Potential Labeling Error
Aidapak Services is recalling Nifedipine 10 mg capsules due to a potential label mixup with multivitamin products.
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 minor labeling errors or low-risk contamination where the probability of serious adverse health consequences is remote.
Plain-English summary
Aidapak Services, LLC is recalling Nifedipine Capsules, 10 mg, NDC 43386044024, due to a labeling error. The recall is issued because the Nifedipine capsules may be potentially mislabeled as Multivitamin/Multimineral w/Fluoride, Chew Tablet, 1 mg (F), NDC 64376081501.
The affected Nifedipine capsules have the pedigree AD23082_7 and an expiration date of 9/23/2013. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the specific NDC and pedigree listed above. If the product matches the description, they should contact their pharmacist or healthcare provider for guidance on how to proceed.
The recalled product
- Product
- NIFEDIPINE Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386044024
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 202
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 (6)
- NIFEDIPINE
- Capsule
- 10 mg has the following codes Pedigree: AD23082_7
- EXP: 9/23/2013
- Pedigree: AD23082_10
- EXP: 9/23/2013.
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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