International safety notice

PrisMax, V2 ROW

Swiss / SwissMedic · CHE · Mar 31, 2022

Key facts

Title PrisMax, V2 ROW
Regulator Swiss / SwissMedic
Country CHE
Brand PrisMax, V2 ROW
Manufacturer Baxter Healthcare SA
Models PrisMax-V3, 3-Entrez, PrisMax-V2, 955558, 955725, 1-Lorsque, 2-Sélectionnez, 4-Sélectionnez, FA-2022-006, 5-Sélectionnez, étape.100
Event type Safety Notice
Date Mar 31, 2022
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices