Nipro Renal Soultions USA, Corporation: Device Recall
Recall #Z-0820-2025 · 11/22/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0820-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Nipro Renal Soultions USA, Corporation
- Status
- Ongoing
- Date Initiated
- 11/22/2024
- Location
- Lewisberry, PA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2,810 units
Reason for Recall
The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Product Description
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Distribution Pattern
US distribution to states of: AZ, FL, GA, GA, IL, MI, NC, NJ, OH, TN, TX.
Other Recalls by Nipro Renal Soultions USA, Corporation
- Class I: Dangerous 04/11/2025
View all recalls by Nipro Renal Soultions USA, Corporation →
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.