Class II

Medical Device Recall: Diasol Acid Concentrate REF G100325-10Dex 100

Diasol, Inc · July 27, 2022

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.

States Affected

NATIONWIDE

Quantity Affected

852 gallon bottles

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0207-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Diasol, Inc Medical Device Recall: Diasol Acid Concentrate REF G100325-10Dex 100 | SafeCheck