Isopure recalls IsoMix PRO systems with Finish Thompson pumps due to possible magnet corrosion from uneven encapsulation. Affected units have specific serial numbers and model numbers. Contact for replacement.
There is a potential for an uneven plastic encapsulation of the magnet ring during the molding process and partial axial displacement. This issue could cause uneven wear during use, cause exposure of the magnet to solution, and thereby result in corrosion and the presence of iron.
Isopure is recalling its IsoMix PRO sodium bicarbonate mixing systems with Finish Thompson centrifugal pumps because a manufacturing defect may cause magnet corrosion. This could lead to contamination of the solution if the magnet is exposed.
The pump's magnet ring may have uneven plastic encapsulation during manufacturing, causing partial axial displacement. This can lead to uneven wear and expose the magnet to the solution, resulting in corrosion and iron contamination.
Users of Isopure's IsoMix PRO systems with Finish Thompson pumps are affected. Those using the system for industrial or laboratory purposes are most at risk due to potential corrosion.
Check for the Finish Thompson Centrifugal Pump Model #110192-3. The IsoMix Pro UDI is (01)008524560:007085 and the serial number starts with IMP-838703.
Reach out to Isopure for replacement or further instructions as the recall remedy is not specified.
The Finish Thompson Centrifugal Pump Model #110192-3.
Check for the Finish Thompson Centrifugal Pump Model #110192-3, IsoMix Pro UDI (01)00852456007085, and serial number starting with IMP-838703.
The recall remedy is not specified, so contact Isopure directly for replacement or further instructions.
We’ve drafted a message you can send Isopure to request your refund or repair — edit it as you like.
Subject: Recall Z-0822-2020 — Isopure Isopure Hello, I own a Isopure that is covered by recall Z-0822-2020 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.
