Isopure Corp recalls ACDS MD704262 acid concentrate storage units for hemodialysis facilities due to potential electrical shock from arching. Affected units have specific serial numbers listed in the recall.
Acidified Concentrate Distribution System potential electrical safety hazard may result in electric shock, arching
Isopure Corp is recalling certain Acidified Concentrate Distribution and Storage (ACDS) units used in hemodialysis facilities because they may cause electric shock or arcing. This could lead to injury if the equipment is not properly maintained.
The ACDS units may cause electrical arcing or shock during normal use, especially if the equipment is not properly maintained or if there are issues with the electrical connections. This could lead to injury if the unit is not functioning safely.
Hemodialysis facility staff and patients who use the recalled ACDS units. Those with the specific serial numbers listed in the recall are most at risk.
Check if your ACDS unit has the model number ACDS MD704262 and one of the listed serial numbers (e.g., AC-869226, AC-869232, etc.). These units are used in hemodialysis facilities for storing and distributing acid concentrate.
Identify the serial number on your ACDS unit to see if it matches the list of affected serial numbers provided in the recall.
Reach out to Isopure Corp directly to confirm if your unit is affected and to get instructions on next steps.
The model number is ACDS MD704262.
Check the serial number on your ACDS unit against the list of affected serial numbers provided in the recall.
Contact Isopure Corp to confirm if your unit is affected and to get instructions on next steps.
We’ve drafted a message you can send Isopure to request your refund or repair — edit it as you like.
Subject: Recall Z-1739-2022 — Isopure Isopure Hello, I own a Isopure that is covered by recall Z-1739-2022 from Isopure. 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.
