Aidapak Recalls Glucosamine/Chondroitin Capsules Due to Potential Label Mixup
Aidapak Services, LLC is recalling Glucosamine/Chondroitin capsules because they may be mislabeled as Fexofenadine HCL tablets.
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, which fits the rubric for moderate severity involving minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling Glucosamine/Chondroitin Capsule, 500 mg/400 mg, Over The Counter, NDC 54458010022. The recall is due to a labeling mixup where the product may be potentially mislabeled as Fexofenadine HCL, Tablet, 60 mg, NDC 45802042578.
The affected product is a 60-capsule bottle with pedigree AD60240_33 and an expiration date of 5/22/2014. 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 the recalling firm for instructions.
The recalled product
- Product
- GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54458010022
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-The-Counter
- 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)
- GLUCOSAMINE/CHONDROITIN
- Capsule
- 500 mg/400 mg has the following code Pedigree: AD60240_33
- 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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