Class II U.S. Food and Drug Administration

Vantive Us Healthcare LLC Primsaflex M100 SET, Product Code 106697 recall: There is a potential dislodgement of the Prismaflex Set deaeration chamber

Recall published 9 months ago

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

The hazard: Device safety concern

The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

What the notice says: There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-1227-2026
Published
February 11, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Vantive Us Healthcare LLC
Product type
Medical devices
Units affected
230,596 units
Distribution
Nationwide
Made in
United States
Lot / code info
UDI/DI 07332414064556, All lots including and manufactured after 24F0077CA
UPC codes
07332414064556

Products covered by this recall

PRIMSAFLEX M100 SET, Product Code 106697; Dialyzer, High Permeability With Or Without Sealed Dialysate System

Check your product

The notice names 3 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 07332414064556

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 596 units

Model or item number

On the rating label, the box or the instruction sheet.

  • 106697

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Vantive Us Healthcare LLC — The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. Ask the supplier or clinic that provided it what the remedy is in your case.
  3. If you are a facility, quarantine affected stock and log the correction.
  4. Report device problems to the FDA through MedWatch.

Who pays for a device recall

The manufacturer funds the remedy. The practical question is usually which link in the chain executes it.

  • If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.
  • Ask for written confirmation that the remedy was applied to your serial number. That is what an insurer or a future clinician will want to see.
  • If you bought it yourself online or from a pharmacy, go to the manufacturer’s recall page rather than the retailer; device claims are handled centrally.
  • Where the remedy is a software update, there is nothing to claim, but do confirm the version changed afterwards.

Company contact: VANTIVE US HEALTHCARE LLC — 510 Lake Cook Rd, Deerfield, IL, 60015-4964

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Vantive Us Healthcare LLC medical devices recalled?

There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 07332414064556; lot code 596 units; model number 106697. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.

Where was the recalled product sold?

It was distributed nationwide.

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