International safety notice

Urgent Field Safety Notice for Oracol+ Saliva Collection Device by Malvern Medical Developments Ltd

Germany / BfArM · DEU · Feb 4, 2022

Key facts

Title Urgent Field Safety Notice for Oracol+ Saliva Collection Device by Malvern Medical Developments Ltd
Regulator Germany / BfArM
Country DEU
Brand Oracol+ Saliva Collection Device
Manufacturer Malvern Medical Developments Ltd
Models 16818, 16753, 16749, 16203, 27.01.2022, 16723, MC333, 16368
Date Feb 4, 2022
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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

Browse all International device safety notices