Vantive US Healthcare recalls Prismaflex HF10:000 Set (Product Code 107142) due to potential dislodgement of the deaeration chamber from the control unit. Affected units include all lots manufactured after 24F0094CA.
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 equipment malfunction during dialysis treatments. Affected units include all lots manufactured after 24F0094CA.
The deaeration chamber in the dialyzer system could become dislodged from the control unit during use. This dislodgement might cause the dialyzer to malfunction, potentially leading to treatment interruptions or complications.
Patients receiving dialysis treatments using the Prismaflex HF1000 Set are most at risk. Healthcare providers who use this equipment for dialysis may also be affected.
Check for the product code 107142 on the Prismaflex HF1000 Set. Affected units were manufactured after the date 24F0094CA and include all lots with the UDI/DI 07332414069315.
Verify the product code 107142 and UDI/DI 07332414069315 on the dialyzer set.
This recall applies to Prismaflex HF1000 Set dialyzers with product code 107142 manufactured after 24F0094CA.
Check for the product code 107142 and UDI/DI 07332414069315 on the dialyzer set. Affected units were manufactured after 24F0094CA.
The recall does not specify a remedy, so contact Vantive US Healthcare for guidance.
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-1230-2026 — Vantive US Healthcare Vantive US Healthcare Hello, I own a Vantive US Healthcare that is covered by recall Z-1230-2026 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.
