Aidapak Recalls Cholecalciferol Capsules Due to Potential Label Mixup
Aidapak Services, LLC is recalling 50,000-unit Cholecalciferol capsules because they may be mislabeled as Fenofibrate tablets. The repacked drugs were distributed in four western states.
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 Cholecalciferol Capsules, 50,000 units, Over The Counter, NDC 53191036201. The recall is due to a labeling error where the product may be mislabeled as Fenofibrate, Tablet, 54 mg, NDC 00378710077. The affected product has the pedigree AD60268_4 and an expiration date of 5/22/2014.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The source text does not specify the exact number of units recalled or the specific retail locations where the product was sold.
Consumers should check their medication for the specific NDC and pedigree listed above. If the product matches the description, they should stop using it and contact their pharmacist or the recalling firm for instructions on return or disposal.
The recalled product
- Product
- CHOLECALCIFEROL Capsule, 50000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 53191036201
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 100
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)
- CHOLECALCIFEROL
- Capsule
- 50000 units has the following code Pedigree: AD60268_4
- EXP: 5/22/2014.
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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