International safety notice

Equipos de diálisis Prismaflex.

Spain / AEMPS · ESP · May 29, 2018

Key facts

Title Equipos de diálisis Prismaflex.
Regulator Spain / AEMPS
Country ESP
Brand Equipos de diálisis Prismaflex.
Manufacturer Gambro Lundia A.B, Suecia
Models 113874, 114489, B-46012696, 86RWJLKDBD, 2018-267, 91.822.52.89, 114870, 96.272.27.95, 28022, 46394, 96.272.28.00, 955052 and 3 more
Event type Safety Notice
Date May 29, 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

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