Diasol recalls 100225-10-DEX100 liquid bicarbonate dialysis concentrate due to unverified safety and efficacy. Affected units have specific lot codes; contact for remedy.
Safety and efficacy of dialysis acid concentrate cannot be assured
Diasol is recalling a specific liquid dialysis concentrate product because its safety and effectiveness cannot be guaranteed. This recall affects patients using the product for dialysis treatments.
The product's safety and efficacy cannot be assured, meaning it might not work properly or could cause harm during dialysis treatments. Without proper testing, the concentrate may not meet medical standards.
Patients using this dialysis concentrate for treatment are most at risk. The recall applies to specific lot codes produced between certain dates.
Check the product label for the lot code PHV07181 through PHV10131. This liquid concentrate is used for bicarbonate dialysis and has a specific 208.2-liter capacity.
Look for the lot code on the label, which should be one of the listed PHV codes.
The recall states the safety and efficacy cannot be assured, so it is not recommended for use.
Affected lot codes range from PHV07181 to PHV10131.
The recall record does not specify a remedy, so contact the manufacturer for assistance.
We’ve drafted a message you can send Diasol to request your refund or repair — edit it as you like.
Subject: Recall Z-0987-2026 — Diasol Diasol Hello, I own a Diasol that is covered by recall Z-0987-2026 from Diasol. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.