Diasol, Inc Diasol Acid Concentrate REF G100325-10Dex 100 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Diasol Acid Concentrate REF G100325-10Dex 100
Brand
Diasol, Inc
Lot Codes / Batch Numbers
Catalog Number: G100325-10Dex100 UDI code: B467100325101004 Lot Number:PHS06011/061722
Products Sold
Catalog Number: G100325-10Dex100 UDI code: B467100325101004 Lot Number:PHS06011/061722
Diasol, Inc is recalling Diasol Acid Concentrate REF G100325-10Dex 100 due to 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.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026