Coenzyme Q-10 Capsules Recalled for Potential Labeling Error
Aidapak Services is recalling Coenzyme Q-10 capsules that may be mislabeled as Pancrelipase DR due to a label mixup.
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 minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling Coenzyme Q-10, Capsule, 30 mg (NDC 00904501546) due to a labeling error. The product may be potentially mislabeled as PANCRELIPASE DR, Capsule, 12000 /38000 /60000 USP units (NDC 00032121201). The affected product has the pedigree W002814 and an expiration date of 6/7/2014.
The repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall is classified as Class II by the FDA, indicating a situation that might temporarily cause or present a slight probability of serious adverse health consequences.
Consumers who have this product should stop using it and contact their pharmacist or the recalling firm for instructions on how to return or dispose of the medication.
The recalled product
- Product
- COENZYME Q-10, Capsule, 30 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904501546
- Manufacturer
- Aidapak Services, LLC
- 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 (4)
- COENZYME Q-10
- Capsule
- 30 mg has the following code Pedigree: W002814
- EXP: 6/7/2014.
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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