Aidapak Recalls Clonazepam Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling clonazepam 0.25 mg tablets that may have been mislabeled as cholecalciferol 2000 units 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 error (label mixup) without reported injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling clonazepam, Tablet, 0.25 mg (1/2 of 0.5 mg), Rx only, NDC 00093083201. The recall is due to a labeling error where the clonazepam tablets may have been mislabeled as cholecalciferol, Capsule, 2000 units, NDC 00536379001.
The affected clonazepam tablets have the pedigree AD73518_1 and an expiration date of 5/31/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for the specific NDC and pedigree codes listed above. If the medication matches the recalled product, they should stop using it and contact their pharmacist or healthcare provider for further instructions.
The recalled product
- Product
- clonazePAM, Tablet, 0.25 mg (1/2 of 0.5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00093083201.
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Prescription Medication
- Hazard
- Affected units
- 200
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)
- clonazePAM
- Tablet
- 0.25 mg (1/2 of 0.5 mg) has the following codes: Pedigree: AD73518_1
- EXP: 5/31/2014.
Distribution
Part of a larger recall action
This product is one of 265 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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