Aidapak Recalls Cranberry Extract Capsules Due to Label Mixup
Aidapak Services is recalling Cranberry Extract/Vitamin C capsules because they may be mislabeled as other medications. The products 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 error (label mixup) without reported illnesses or injuries, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling 546-capsule bottles of Cranberry Extract/Vitamin C Capsule, 450 mg/125 mg, Over The Counter. The recall is due to a labeling error where the product may be mislabeled as other drugs, including Multivitamin/Multimineral, Modafinil, Niacin ER, or Glucosamine/Chondroitin.
The affected products were distributed in Arizona, California, Oregon, and Washington. Specific pedigree codes and expiration dates are listed in the official recall notice.
Consumers should check their medication labels and stop using the product if it matches the description. They should contact their pharmacist or the recalling firm for instructions on returning the product.
The recalled product
- Product
- CRANBERRY EXTRACT/VITAMIN C Capsule, 450 mg/125 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 31604014271
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 546
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 (11)
- CRANBERRY EXTRACT/VITAMIN C Capsule
- 450 mg/125 mg has the following codes Pedigree: W002692
- EXP: 6/5/2014
- Pedigree: W003715
- EXP: 6/26/2014
- Pedigree: W003716
- Pedigree: AD60240_11
- EXP: 5/22/2014
- Pedigree: W002693
- Pedigree: AD46257_13
- EXP: 5/15/2014.
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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