---
title: "Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25 — FDA record Z-0820-2025 | Is It on Recall"
description: "The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca."
url: https://isitonrecall.com/recall/fda-device-z-0820-2025-citric-complete-dry-citric-acid-concentrate-model-number-dca-225-25/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0820-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0820-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Nipro Renal Soultions USA, Corporation records](https://isitonrecall.com/brand/nipro-renal-soultions-usa-corporation/)