Magnesium Citrate Oral Solution Recalled for Bacterial Contamination
Pharma Nobis LLC is recalling 7,404 bottles of Freskaro Magnesium Citrate Oral Solution nationwide due to the presence of Acetobacter nitrogenifigens bacteria.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Microbial contamination of a pharmaceutical oral solution represents a risk-of-harm to consumers. No illnesses or injuries have been reported, which limits the classification to High (Score 3) rather than Severe or Critical per FDA guidelines.
Plain-English summary
Pharma Nobis LLC is recalling Freskaro Magnesium Citrate Oral Solution (Cherry flavor, 10 fl. oz) due to microbial contamination. The affected product is Lot A80622 with an expiration date of 11/2025. A total of 7,404 bottles have been distributed nationwide.
The recall was initiated due to the presence of Acetobacter nitrogenifigens bacteria in this non-sterile product. This is an FDA Class II recall.
Consumers who have purchased this product should stop using it and contact Pharma Nobis LLC or a healthcare provider with any questions or concerns.
The recalled product
- Product
- MAGNESIUM CITRATE (FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - CHERRY)
- Brand
- MAGNESIUM CITRATE
- Manufacturer
- Pharma Nobis LLC
- Category
- Drug — Oral Laxative
- Affected units
- 7,404
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 A80622
- Exp. 11/2025
UPCs (1)
- 0382645312107
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.
See all 5 products in this recall →Related recalls
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