International safety notice

Urgent Field Safety Notice for AquaPak 340 ml by Teleflex Medical Morrisville

Germany / BfArM · DEU · Apr 20, 2023

Key facts

Title Urgent Field Safety Notice for AquaPak 340 ml by Teleflex Medical Morrisville
Regulator Germany / BfArM
Country DEU
Brand AquaPak 340 ml
Manufacturer Teleflex Medical Morrisville
Models EIF-000532, APRIL-2023, 400340, 228327, D-47533, 228237, 22B327, PADLU¢9, 8ENACHRICHTIGUNG, 8ITTE, FSCA-23
Date Apr 20, 2023
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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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