Cilostazol Tablets Recalled for Potential Labeling Mixup with Dutasteride
Aidapak Services is recalling Cilostazol 100 mg tablets because they may be mislabeled as Dutasteride 0.5 mg capsules.
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 between two different prescription drugs. This fits the rubric for moderate severity, as it is a labeling error without reported injuries or deaths.
Plain-English summary
Aidapak Services, LLC is recalling Cilostazol Tablet, 100 mg, NDC 60505252201, due to a labeling mixup. The recalled product may be potentially mislabeled as Dutasteride, Capsule, 0.5 mg, NDC 00173071204.
The affected product is identified by the pedigree AD65475_4 and an expiration date of 5/28/2014. 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 stop using it and contact their pharmacist or healthcare provider for further instructions.
The recalled product
- Product
- CILOSTAZOL Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505252201
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 60
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)
- CILOSTAZOL Tablet
- 100 mg has the following code Pedigree: AD65475_4
- EXP: 5/28/2014.
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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