Class II — Diasol, Inc
| Recalling firm | DIASOL, INC. |
|---|---|
| Registered facility | DIASOL INC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Incorrect labeling of dialysate concentration for hemodialysis. |
| Product | DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS |
| Quantity | 212 Cases of 4 gallons each |
| Distribution | U.S.: CA O.U.S.:None |
| Initiated | 2020-04-30 |
| Classified | 2020-06-18 |
| Terminated | 2024-05-28 |
| Recall number | Z-2402-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Diasol, Inc (Z-2402-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85695/
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