FDA DevicesClass II
PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or Wi...
Published: February 11, 2026Recall ID: Z-1228-2026Category: devicesCountry: US
Reason for Recall / Hazard
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
Product Description & Identification
PRISMAFLEX M150 SET, Product Code 109990; Dialyzer, High Permeability With Or Without Sealed Dialysate System
Additional Source Details
| Field | Value |
|---|---|
| City | Deerfield |
| State | IL |
| Event id | 98180 |
| Address 1 | 510 Lake Cook Rd |
| Address 2 | N/A |
| Code info | UDI/DI 07332414090005, All lots including and manufactured after 24F0100CA |
| Postal code | 60015-4964 |
| Report date | 20260211 |
| Product type | Devices |
| Product quantity | 137,576 units |
| Reason for recall | There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260106 |
| Initial firm notification | Letter |
| Center classification date | 20260202 |
Overview
- Recalling FirmVANTIVE US HEALTHCARE LLC
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution.