Vantive US Healthcare recalls Prismaflex HF10:000 Set (Product Code 107140) due to potential dislodgement of deaeration chamber from control unit. Affected units include all lots manufactured after 24G0034CA.
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
Vantive US Healthcare is recalling Prismaflex HF1000 Set dialyzers because the deaeration chamber might detach from the control unit. This could lead to improper dialysis treatment if the chamber becomes dislodged during use.
The deaeration chamber in the Prismaflex Set could become dislodged from the control unit during use. This dislodgement might cause improper dialysis treatment, potentially leading to health complications for patients.
Healthcare professionals using the Prismaflex HF1000 Set for hemodialysis are most at risk. Patients receiving dialysis through this equipment may be affected if the set is used without proper installation.
Check for the product code 107140 on the Prismaflex HF1000 Set. Affected units include all lots manufactured after 24G0034CA.
Look for product code 107140 on the Prismaflex HF1000 Set.
Contact Vantive US Healthcare for further instructions on the recall.
The recall is for potential dislodgement of the deaeration chamber from the control unit, which could lead to improper dialysis treatment. However, the remedy does not specify immediate action to stop use.
Check the product code 107140 and contact Vantive US Healthcare for further instructions on the recall.
All lots of the Prismaflex HF1000 Set manufactured after 24G0034CA are affected.
We’ve drafted a message you can send Vantive US Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1229-2026 — Vantive US Healthcare Vantive US Healthcare Hello, I own a Vantive US Healthcare that is covered by recall Z-1229-2026 from Vantive US Healthcare. 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.
