Magnesium Chloride Tablets Recalled for Potential Label Mixup
Aidapak Services is recalling Magnesium Chloride tablets that may be mislabeled as Selegiline HCL or Phosphorus due to a label mixup.
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 minor labeling errors or low-risk contamination.
Plain-English summary
Aidapak Services, LLC is recalling specific lots of Magnesium Chloride DR, Tablet, 64 mg, Over The Counter. The recall is due to a labeling error where the product may be potentially mislabeled as Selegiline HCL, Capsule, 5 mg, or Phosphorus, Tablet, 250 mg.
The affected product is distributed in Arizona, California, Oregon, and Washington. The recall involves two specific pedigree codes: AD54510_1 and AD70615_1, both with an expiration date of 2/28/2014. The mislabeling risk involves products with pedigree AD54549_19 (expiring 5/20/2014) and AD70639_10 (expiring 5/29/2014).
Consumers should check their medication labels for the NDC 00904791152 and the specific pedigree codes listed above. If the product matches the recalled description, consumers should stop using it and contact their pharmacist or the recalling firm for instructions on return or replacement.
The recalled product
- Product
- MAGNESIUM CHLORIDE DR, Tablet, 64 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904791152
- Manufacturer
- Aidapak Services, LLC
- Category
- Drug — Over-the-Counter
- 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 (6)
- MAGNESIUM CHLORIDE DR
- Tablet
- 64 mg has the following codes Pedigree: AD54510_1
- EXP: 2/28/2014
- Pedigree: AD70615_1
- EXP: 2/28/2014.
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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