Vantive Healthcare recalls Prismaflex ST150 dialyzer sets due to potential dislodgement of deaeration chamber from control unit. Affected units include all lots manufactured after 24F0085.
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
Vantive Healthcare is recalling Prismaflex ST150 dialyzer sets because the deaeration chamber might detach from the control unit. This could cause serious injury during dialysis treatments if the chamber becomes dislodged.
The deaeration chamber in the dialyzer set could become dislodged from the control unit during dialysis. This dislodgement might lead to complications if the chamber separates from the system while the patient is connected.
Patients receiving dialysis treatments using the recalled Prismaflex ST150 sets are most at risk. Healthcare providers using these sets for dialysis also need to take action.
Check for the product code 107640US on the dialyzer set. The affected units were manufactured after 24F0085 and include all lots with UDI/DI 00085412917696.
Look for product code 107640US on the dialyzer set.
Contact Vantive Healthcare for specific instructions on how to handle the recalled set.
The recall indicates a potential dislodgement of the deaeration chamber from the control unit, which could cause serious injury during dialysis. However, the remedy does not specify immediate action to stop use.
The official recall notice does not provide specific action steps for affected users beyond checking the product code and contacting Vantive Healthcare.
All lots manufactured after 24F0085 are affected, including those with UDI/DI 00085412917696.
We’ve drafted a message you can send Vantive Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1225-2026 — Vantive Healthcare Vantive Healthcare Hello, I own a Vantive Healthcare that is covered by recall Z-1225-2026 from Vantive 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.
