International safety notice

Sistemas de infusión CME/BD BodyGuard ™ Microset/Bodyset; Bombas de infusión de gran volumen CME/BD BodyGuard™.

Spain / AEMPS · ESP · Aug 31, 2021

Key facts

Title Sistemas de infusión CME/BD BodyGuard ™ Microset/Bodyset; Bombas de infusión de gran volumen CME/BD BodyGuard™.
Regulator Spain / AEMPS
Country ESP
Brand Sistemas de infusión CME/BD BodyGuard ™ Microset/Bodyset; Bombas de infusión de gran volumen CME/BD BodyGuard™.
Manufacturer Caesarea Medical Electronics Limited, Reino Unido
Models A120-003XS2YV, GEN00007, 28022, PCA00013, ONC00010, GEN00005, 100-163XESVK, ONC00004, 101-163XESK, ONC00006, PCA00004, 71717 and 80 more
Event type Safety Notice
Date Aug 31, 2021

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