International safety notice

Bombas de infusión ambulatoria CADD® Solis VIP, Referencias: 21-2120-0105-02L, 21-2120-0105-03L, 21-2120-0105-06L, 21-2120-0105-07L, 21-2120-0105-08L, 21-2120-0105-12L, 21-2120-0105-13L, 21-2120-0105-14L, 21-2120-0105-15L, 21-2120-0105-17L, 21-2120-0105-5

Spain / AEMPS · ESP · Mar 30, 2020

Key facts

Title Bombas de infusión ambulatoria CADD® Solis VIP, Referencias: 21-2120-0105-02L, 21-2120-0105-03L, 21-2120-0105-06L, 21-2120-0105-07L, 21-2120-0105-08L, 21-2120-0105-12L, 21-2120-0105-13L, 21-2120-0105-14L, 21-2120-0105-15L, 21-2120-0105-17L, 21-2120-0105-5
Regulator Spain / AEMPS
Country ESP
Brand Bombas de infusión ambulatoria CADD® Solis VIP, Referencias: 21-2120-0105-02L, 21-2120-0105-03L, 21-2120-0105-06L, 21-2120-0105-07L, 21-2120-0105-08L, 21-2120-0105-12L, 21-2120-0105-13L, 21-2120-0105-14L, 21-2120-0105-15L, 21-2120-0105-17L, 21-2120-0105-5
Manufacturer Smiths Medical ASD, Inc., Estados Unidos
Models 91.822.52.89, 21-2120-0105-50L, 28022, 21-2120-0105-03L, 2127-0105-06L, 21-2120-0105-06L, 21-2120-0105-5, 21-2120-0105-17L, 21-2120-0105-13L, 2020-005-R, 21-2127-0105-06L, 21-2120-0105-02L and 13 more
Event type Safety Notice
Date Mar 30, 2020

At a glance

  • No Recall
  • Yes Field safety notice

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