Multivitamin Chew Tablets Recalled for Potential Labeling Mixup
Aidapak Services is recalling Multivitamin/Multimineral Chew Tablets because they may be mislabeled as Levothyroxine Sodium or Lactobacillus Acidophilus.
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 illness fall under the Moderate severity category.
Plain-English summary
Aidapak Services, LLC is recalling 180-count bottles of Multivitamin/Multimineral Chew Tablets (NDC 58914001460). The recall is due to a labeling mixup where the product may be potentially mislabeled as Levothyroxine Sodium, Tablet, 12.5 mcg (NDC 00527134101) or Lactobacillus Acidophilus, Capsule, 500 Million CFU (NDC 43292050022).
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The specific pedigree codes for the recalled multivitamin are AD30180_10 and AD32325_1, both with an expiration date of 5/9/2014. The source text does not report any illnesses or injuries associated with this recall.
Consumers should check their medication bottles for the NDC 58914001460 and the pedigree codes listed above. If the product matches these details, consumers should stop using it and contact their pharmacist or the recalling firm for instructions on return or disposal.
The recalled product
- Product
- MULTIVITAMIN/MULTIMINERAL Chew Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 58914001460
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 180
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 (5)
- MULTIVITAMIN/MULTIMINERAL
- Chew Tablet has the following codes Pedigree: AD30180_10
- EXP: 5/9/2014
- Pedigree: AD32325_1
- EXP: 5/9/2014.
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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