# FDA recall Z-0820-2025

> **Nipro Renal Soultions USA, Corporation** · Class II · device recall initiated 2024-11-22.

## Product

Citric Complete - Dry Citric Acid Concentrate  Model Number: DCA+225-25

## 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.

## Key facts

- **Recall number:** Z-0820-2025
- **Recalling firm:** Nipro Renal Soultions USA, Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-22
- **Report date:** 2025-01-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lewisberry, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0820-2025

## Citation

> AI Analytics. FDA recall Z-0820-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0820-2025. Source: US FDA. Licensed CC0.

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