# FDA recall Z-0207-2025

> **Diasol, Inc** · Class II · device recall initiated 2022-07-27.

## Product

Diasol Acid Concentrate  REF G100325-10Dex 100

## Reason for recall

Due to labeling issue.  The box label is different that the gallon label in that gallon label shows a lower Calcium concentration than the box label.

## Distribution

U.S. Nationwide distribution in the state of AZ.

## Key facts

- **Recall number:** Z-0207-2025
- **Recalling firm:** Diasol, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-27
- **Report date:** 2024-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Phoenix, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0207-2025

## Citation

> AI Analytics. FDA recall Z-0207-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0207-2025. Source: US FDA. Licensed CC0.

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