Aidapak Recalls Multivitamin Tablets Due to Potential Labeling Errors
Aidapak Services, LLC is recalling multivitamin tablets that may be mislabeled as quetiapine or docusate sodium. The recall covers specific lots 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 mixup. Per the rubric, minor labeling errors and voluntary precautionary recalls without reported injuries are rated as Moderate.
Plain-English summary
Aidapak Services, LLC is recalling 1,045 tablets of Multivitamin/Multimineral, Over The Counter, NDC 37205018581. The recall is due to a labeling mixup where the product may be potentially mislabeled as Quetiapine Fumarate, Tablet, 25 mg, or Docusate Sodium, Capsule, 250 mg.
The affected lots include Pedigree AD32328_8 with an expiration date of 5/9/2014, and Pedigree W002513 with an expiration date of 6/3/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication for these specific pedigree codes and expiration dates. If the product matches the description, they should stop using it and contact their pharmacist or the recalling firm for instructions on disposal or replacement.
The recalled product
- Product
- MULTIVITAMIN/MULTIMINERAL Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 37205018581
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-The-Counter
- Hazard
- Affected units
- 1,045
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)
- MULTIVITAMIN/MULTIMINERAL Tablet has the following codes Pedigree: AD32328_8
- EXP: 5/9/2014
- Pedigree: W002513
- EXP: 6/3/2014.
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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