Recall archive / FDA device enforcement
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25 — FDA record Z-0820-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 22, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
- Reason
- The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
- Classification
- Class II
- Recalling firm
- Nipro Renal Soultions USA, Corporation
- Quantity
- 2,810 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0820-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Model Number: DCA+225-25. Lot Numbers: NDC4F001, NDC4G006, NDC4H009, NDC4H010. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US distribution to states of: AZ, FL, GA, GA, IL, MI, NC, NJ, OH, TN, TX.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jan 15, 2025
- Recall initiation date
- Nov 22, 2024
- Center classification date
- Jan 8, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.