FDA Device recall Z-0207-2025
Diasol Acid Concentrate REF G100325-10Dex 100
- FDA Device
- Class II
- ongoing
- Published 2024-10-30
On 2024-10-30 the FDA classified a Class II recall of Diasol Acid Concentrate REF G100325-10Dex 100 by Diasol, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0207-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-07-27 |
| Published | 2024-10-30 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Diasol |
| Distribution | US |
Product
Diasol Acid Concentrate REF G100325-10Dex 100
Reason
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.
Identifiers
| code_info | Catalog Number: G100325-10Dex100 UDI code: B467100325101004 Lot Number:PHS06011/061722 |
|---|
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-0207-2025%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.