Sodium Chloride Tablets Recalled for Potential Labeling Mixup
Aidapak Services is recalling 7,891 sodium chloride tablets that may have been mislabeled as other drugs due to a labeling error.
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 injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Aidapak Services, LLC is recalling 7,891 tablets of Sodium Chloride, 1 mg, Over The Counter (NDC 00223176001). The recall is due to a labeling mixup where the product may have been mislabeled as other medications, including Bisacodyl EC, Dutasteride, or Omega-3 Fatty Acid.
The affected repacked drugs were distributed in Arizona, California, Oregon, and Washington. The recall involves specific pedigree codes and expiration dates ranging from May 2, 2014, to June 27, 2014.
Consumers should check their medication for the specific NDC and pedigree codes listed in the recall notice. If the product matches the description, they should stop using it and contact their pharmacist or the recalling firm for instructions.
The recalled product
- Product
- SODIUM CHLORIDE, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00223176001.
- Manufacturer
- Aidapak Services, LLC
- Hazard
- Affected units
- 7,891
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 (18)
- SODIUM CHLORIDE
- Tablet
- 1 mg has the following codes: Pedigree: AD39560_1
- EXP: 5/13/2014
- Pedigree: AD70636_1
- EXP: 5/29/2014
- Pedigree: AD73662_1
- EXP: 6/3/2014
- Pedigree: W002611
- EXP: 6/4/2014
- Pedigree: W003792
- EXP: 6/27/2014
- Pedigree: AD22845_10
- EXP: 5/2/2014
- Pedigree: W003115
- EXP: 6/13/2014
- Pedigree: W003707
- EXP: 6/25/2014.
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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