Aidapak Recalls D-Alpha Tocopheryl Acetate Capsules Due to Labeling Error
Aidapak Services, LLC is recalling D-Alpha Tocopheryl Acetate capsules because they may be mislabeled as Cyanocobalamin 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 without reported injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling D-Alpha Tocopheryl Acetate Capsules, 400 units, Over The Counter, NDC 49348041010. The recall is due to a labeling error where the product may be mislabeled as CYANOCOBALAMIN, Tablet, 500 mcg, NDC 00536355101.
The affected product is identified by Pedigree AD52993_28 and an expiration date of 5/20/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication labels and discontinue use if the product matches the recalled description. The FDA classifies this as a Class II recall.
The recalled product
- Product
- D-ALPHA TOCOPHERYL ACETATE Capsule, 400 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348041010
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-The-Counter
- Hazard
- Affected units
- 107
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)
- D-ALPHA TOCOPHERYL ACETATE
- Capsule
- 400 units has the following code Pedigree: AD52993_28
- EXP: 5/20/2014.
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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