International safety notice

Sistemas de anestesia:  Flow-i, Referencias 6677200, 6677300, 6677400, 6888520, 6888530, 6888540  Flow-c, Referencia 6887700  Flow-e, Referencia 6887900

Spain / AEMPS · ESP · Dec 28, 2023

Key facts

Title Sistemas de anestesia:  Flow-i, Referencias 6677200, 6677300, 6677400, 6888520, 6888530, 6888540  Flow-c, Referencia 6887700  Flow-e, Referencia 6887900
Regulator Spain / AEMPS
Country ESP
Brand Sistemas de anestesia:  Flow-i, Referencias 6677200, 6677300, 6677400, 6888520, 6888530, 6888540  Flow-c, Referencia 6887700  Flow-e, Referencia 6887900
Manufacturer Maquet Critical Care AB, Suecia.
Models 6677300, 6677200, 6888520, 6887900, 6.1-6.2, MCC_23_002_IU, 91.822.52.89, 6887700FLOW-E, 100716, 6888530, 6887700, 6888540 and 7 more
Event type Safety Notice
Date Dec 28, 2023

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