International safety notice

Sistemas de anestesia Flow: -Flow-c, referencia: 68 87 700 -Flow-e, referencia: 68 87 900 -Flow-i C20, referencia: 68 88 520 -Flow-i C30, referencia: 68 88 530 -Flow-i C40, referencia: 68 88 540

Spain / AEMPS · ESP · Nov 17, 2022

Key facts

Title Sistemas de anestesia Flow: -Flow-c, referencia: 68 87 700 -Flow-e, referencia: 68 87 900 -Flow-i C20, referencia: 68 88 520 -Flow-i C30, referencia: 68 88 530 -Flow-i C40, referencia: 68 88 540
Regulator Spain / AEMPS
Country ESP
Brand Sistemas de anestesia Flow: -Flow-c, referencia: 68 87 700 -Flow-e, referencia: 68 87 900 -Flow-i C20, referencia: 68 88 520 -Flow-i C30, referencia: 68 88 530 -Flow-i C40, referencia: 68 88 540
Manufacturer Maquet Critical Care AB, Suecia.
Models 91.822.52.89, 86840, 28521, MX-8732, 20002, MCC-22-009-NU, 530FLOW-I, 50148, 520FLOW-I, 20001, 2022-508, U2823494 and 12 more
Event type Safety Notice
Date Nov 17, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 100–999 Matching device models in FDA data
  • 100–999 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