FDA Device recall Z-0820-2025
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
- FDA Device
- Class II
- ongoing
- Published 2025-01-15
On 2025-01-15 the FDA classified a Class II recall of Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25 by Nipro Renal Soultions Usa, citing the outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0820-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-11-22 |
| Published | 2025-01-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Nipro Renal Soultions Usa |
| Distribution | AZ, FL, GA, IL, MI, NC, NJ, OH, TN, TX |
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.
Identifiers
| code_info | Model Number: DCA+225-25. Lot Numbers: NDC4F001, NDC4G006, NDC4H009, NDC4H010. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0820-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.