Diasol Acid Concentrate REF G100325-10Dex 100 — Class II medical device recall Z-0207-2025
Ongoing recall by Diasol, Inc, reported 2024-10-30, distributed nationwide. Due to labeling issue. The box label is different that the gallon label in that gallon label shows a lower Cal
| Recall number | Z-0207-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Diasol, Inc, Phoenix, AZ, United States |
| Recall initiated | 2022-07-27 |
| Classified | 2024-10-23 |
| Reported by FDA | 2024-10-30 |
| Distributed | Nationwide (US) |
| Quantity | 852 gallons |
| Reason classes | labeling |
| Lot numbers | PHS06011/061722 |
| Model numbers | 100, G100325-10DEX, G100325-10DEX100 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0207-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.