International safety notice

Cardiosave Hybrid y Cardiosave Rescue (Fabricados desde diciembre de 2011).

Spain / AEMPS · ESP · Apr 15, 2024

Key facts

Title Cardiosave Hybrid y Cardiosave Rescue (Fabricados desde diciembre de 2011).
Regulator Spain / AEMPS
Country ESP
Brand Cardiosave Hybrid y Cardiosave Rescue (Fabricados desde diciembre de 2011).
Manufacturer Datascope Corp. Getinge, EEUU.
Models 10607567113432, 10607567108414N, 0998-00-0800-65, 10607567111117, 10607567109053N, 10607567108438N, A786SAA3F8, 0998-00-0800-85, 28521, 38280, 2022-001-C, 10607567109008N and 44 more
Event type Safety Notice
Date Apr 15, 2024

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