RegWardenFDA facility compliance records
Recall

Class II — Diasol, Inc

Recalling firmDIASOL, INC.
Registered facilityDIASOL INC (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonDue 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.
ProductDiasol Acid Concentrate REF G100325-10Dex 100
Quantity852 gallon bottles
DistributionU.S. Nationwide distribution in the state of AZ.
Initiated2022-07-27
Classified2024-10-23
Recall numberZ-0207-2025
InitiationVoluntary: 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-0207-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/95334/

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