Diasol Acid Concentrate REF G100325-10Dex 100
FDA Recall Z-0207-2025 · Posted 2024-10-23
Recalling FirmDiasol, Inc
Recall StatusOpen, Classified
Product CodeKPO
Date Initiated2022-07-27
Product Quantity852 gallon bottles
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.
Firm Action
On 07/26/2022, the firm communicated via email with customer that 2 case were incorrectly labeled. Cases marked 3K 2.5ca have inside box label as 3K 2.0ca. Customer was instructed not to use the product and the firm picked up mislabeled product.
Root Cause
Labeling mix-ups
Distribution Pattern
U.S. Nationwide distribution in the state of AZ.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.