International safety notice

Kit de aguja para biopsia pasiva, modelo 9733068 y Kit FPU para biopsia pasiva, modelo 9731754

Spain / AEMPS · ESP · Nov 13, 2019

Key facts

Title Kit de aguja para biopsia pasiva, modelo 9733068 y Kit FPU para biopsia pasiva, modelo 9731754
Regulator Spain / AEMPS
Country ESP
Brand Kit de aguja para biopsia pasiva, modelo 9733068 y Kit FPU para biopsia pasiva, modelo 9731754
Manufacturer Medtronic Navigation Inc, Estados Unidos
Models 08820, 066535518, 9733068KIT, 0009709452, 28022, 2019-598, 066512319A, 91.822.52.89, 066535518A, 55751, 066529218, 066513519A and 18 more
Event type Safety Notice
Date Nov 13, 2019

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models 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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