Freskaro Magnesium Citrate oral solution recalled for bacterial contamination
Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor) nationwide due to the presence of Acetobacter nitrogenifigens bacteria.
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: FDA Class II recall with no reported illnesses or hospitalizations. Acetobacter nitrogenifigens is not a high-risk pathogen, and the absence of reported illness cases places this in the Moderate severity category.
Plain-English summary
Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Grape Flavor), an over-the-counter saline laxative, due to the presence of Acetobacter nitrogenifigens bacteria. The affected lot is A80553 with an expiration date of November 2025. Approximately 53,268 bottles were distributed nationwide.
This is an FDA Class II recall, which indicates a serious potential health hazard. The recall addresses microbial contamination in this non-sterile product.
Consumers with questions about this recall should contact Pharma Nobis LLC or the FDA.
The recalled product
- Product
- MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE)
- Brand
- MAGNESIUM CITRATE
- Manufacturer
- Pharma Nobis LLC
- Category
- Drug — Saline Laxative
- Affected units
- 53,268
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 (2)
- Lot A80553
- Exp. 11/2025
UPCs (1)
- 0382645311100
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 5 recalled by Pharma Nobis 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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