Aidapak Recalls Aspirin EC Tablets Due to Potential Label Mixup
Aidapak Services, LLC is recalling Aspirin EC DR tablets because they may be mislabeled as Melatonin or Docusate Sodium.
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 (mislabeling) without reported illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Aidapak Services, LLC is recalling 544 tablets of Aspirin EC DR, 81 mg, Over The Counter (NDC 49348098015). The recall is due to a labeling error where the product may be potentially mislabeled as Melatonin, Tablet, 3 mg (NDC 51991001406) or Docusate Sodium, Capsule, 250 mg (NDC 0090478915).
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The specific pedigree codes for the recalled Aspirin are AD28349_1 and W003672, both with an expiration date of 2/28/2014.
Consumers should check their medication for the NDC 49348098015 and the pedigree codes listed above. If the product matches these details, it should be returned to the pharmacy or point of purchase for a refund or replacement.
The recalled product
- Product
- ASPIRIN EC DR Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348098015
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 544
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 (6)
- ASPIRIN EC DR
- Tablet
- 81 mg has the following codes Pedigree: AD28349_1
- EXP: 2/28/2014
- Pedigree: W003672
- EXP: 2/28/2014.
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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