International safety notice

Consolas de contrapulsación intra-aórtica (IABP): IABP Cardiosave Hybrid, referencia 0998-00-0800-XX y IABP Cardiosave Rescue, referencia 0998-UC-0800-XX

Spain / AEMPS · ESP · Nov 2, 2018

Key facts

Title Consolas de contrapulsación intra-aórtica (IABP): IABP Cardiosave Hybrid, referencia 0998-00-0800-XX y IABP Cardiosave Rescue, referencia 0998-UC-0800-XX
Regulator Spain / AEMPS
Country ESP
Brand Consolas de contrapulsación intra-aórtica (IABP): IABP Cardiosave Hybrid, referencia 0998-00-0800-XX y IABP Cardiosave Rescue, referencia 0998-UC-0800-XX
Manufacturer Maquet, EEUU
Models 250–3, 0070-00-0638-20, 7.12.1, 0070-00-0637-07, 381M~975M, 2018-561, 0070-00-0638-15, 0070-00-0638-17, 795–676, 060HPA~901HPA), 0070-00-0638-03, 060–901 and 73 more
Event type Safety Notice
Date Nov 2, 2018

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