Nipro Renal Solutions USA has recalled approximately 2,810 units of Citric Complete Dry Citric Acid Concentrate (Model DCA+225-25) because the outer shipping cases are mislabeled. The packaging incorrectly lists the potassium and calcium levels as 3.0 K and 2.0 Ca, when the product actually contains 2.0 K and 3.0 Ca. No incidents or injuries have been reported to date.
The mislabeling of electrolyte concentrations could lead to patients receiving the wrong levels of potassium and calcium during dialysis treatment. This discrepancy could potentially cause serious health complications associated with electrolyte imbalances if healthcare providers rely on the incorrect label for treatment settings.
Recall #: Z-0820-2025
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
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Sources: FDA iRES · Raw API Response
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