International safety notice

Bomba de contrapulsación intraaórtica AutoCAT®2, Bomba de contrapulsación intraaórtica AC3 Optimus®

Spain / AEMPS · ESP · Jan 10, 2023

Key facts

Title Bomba de contrapulsación intraaórtica AutoCAT®2, Bomba de contrapulsación intraaórtica AC3 Optimus®
Regulator Spain / AEMPS
Country ESP
Brand Bomba de contrapulsación intraaórtica AutoCAT®2, Bomba de contrapulsación intraaórtica AC3 Optimus®
Manufacturer Arrow International LLC , EE UU.
Models EIF-000522-01, IAP-0701, AUTOCAT®2, IAP-0500SV, IAP-0535J, 2022-545-CORREGIDA, IAP-0500J, IAP-0400J, IAP-0500F, IAP-0400, IAP-0400F, IAP-0500I and 24 more
Event type Safety Notice
Date Jan 10, 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