Class II
Medical Device Recall: Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Nipro Renal Soultions USA, Corporation · November 22, 2024
Reason for Recall
The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Distribution
US distribution to states of: AZ, FL, GA, GA, IL, MI, NC, NJ, OH, TN, TX.
States Affected
AZ, FL, GA, IL, MI, NC, NJ, OH, TN, TX
Quantity Affected
2,810 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0820-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.