International safety notice

Ureteral Stent

Swiss / SwissMedic · CHE · Nov 21, 2022

Key facts

Title Ureteral Stent
Regulator Swiss / SwissMedic
Country CHE
Brand Ureteral Stent
Manufacturer Teleflex Medical
Models 71F19K3067, 71F19H2189, 71F18A2134, 71F19F1466, 71F18A2124, 71F21M0136, 71F17M0214, 71F19M0529, 71F21F0196, 71F19G0933, 71F18G1086, 71F18H0195 and 1890 more
Event type Safety Notice
Date Nov 21, 2022
Regulator page fsca.swissmedic.ch

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

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