Diasol, Inc recalls Brand Name: Diasol Product Name: 100225-10-DEX100
- Recalling company
- Diasol, Inc
- Product
- Brand Name: Diasol Product Name: 100225-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0CA, 1.0MG, 208.2 liters
- Reason
- Safety and efficacy of dialysis acid concentrate cannot be assured
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Nov 5, 2025
- Reported
- Dec 31, 2025
- Distribution
- US Nationwide distribution in the states of MO, CA, AZ, TX, IL, MA.
- Status
- Ongoing
- Quantity
- 186,000 containers
- Lot / codes
- UDI: None; Lot Code: PHV07181 PHV07211 PHV07231 PHV07251 PHV07281 PHV07282 PHV07301 PHV07302 PHV07311 PHV08011 PHV08041 PHV08051 PHV08061 PHV08071 PHV08111 PHV08121 PHV08131 PHV08132 PHV08141 PHV08151 PHV08181 PHV08251 PHV08252 PHV09021 PHV09041 PHV09081 PHV09091 PHV09121 PHV09151 PHV09161 PHV09181 PHV09191 PHV09221 PHV09231 PHV09291 PHV10031 PHV10061 PHV10081 PHV10091 PHV10131
- Company location
- Phoenix, AZ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0987-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0987-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.