Lactobacillus Acidophilus Tablets Recalled for Potential Labeling Error
Aidapak Services, LLC is recalling Lactobacillus Acidophilus tablets because they may have been mislabeled as Repaglinide.
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 (label mixup) without reported injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Aidapak Services, LLC is recalling Lactobacillus Acidophilus, Tablet, 35 MILLION, Over The Counter, NDC 00536718101. The recall is due to a labeling error where the product may have been mislabeled as Repaglinide, Tablet, 1 mg, NDC 00169008281.
The affected product is identified by Pedigree W003865 and an expiration date of 6/27/2014. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Consumers should check their medication labels for the specific NDC and pedigree codes listed above. If the product matches the description, consumers should stop using it and contact their pharmacist or healthcare provider for guidance.
The recalled product
- Product
- LACTOBACILLUS ACIDOPHILUS, Tablet, 35 MILLION, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536718101.
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 100
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)
- LACTOBACILLUS ACIDOPHILUS
- Tablet
- 35 MILLION has the following codes: Pedigree: W003865
- EXP: 6/27/2014.
Distribution
Part of a larger recall action
This product is one of 265 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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