Lactobacillus Tablets Recalled for Potential Labeling Errors
Aidapak Services, LLC is recalling Lactobacillus tablets due to a label mixup that may cause them to be mislabeled as other medications.
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 1,249 Lactobacillus tablets (NDC 64980012950) because of a labeling error. The agency identified a label mixup where the Lactobacillus tablets may be potentially mislabeled as other products, including Multivitamin/Multimineral tablets, Calcium Acetate capsules, Lithium Carbonate ER tablets, and Omega-3 Fatty Acid capsules.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall involves specific pedigree codes and expiration dates, including AD62986_10, AD62992_1, AD22865_1, W003624, W003622, and W003623.
Consumers should check their medication labels and stop using the product if it matches the recalled description. They should contact their healthcare provider or pharmacist for guidance on proper disposal or replacement.
The recalled product
- Product
- LACTOBACILLUS Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980012950
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-the-Counter
- Hazard
- Affected units
- 1,249
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 (11)
- LACTOBACILLUS Tablet has the following codes Pedigree: AD62986_10
- EXP: 5/23/2014
- Pedigree: AD62992_1
- Pedigree: AD22865_1
- EXP: 5/2/2014
- Pedigree: W003624
- EXP: 1/31/2014
- Pedigree: W003622
- EXP: 6/25/2014
- Pedigree: W003623
- EXP: 10/31/2013.
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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