International safety notice

VaccZyme™ Human Anti-Haemophilus Influenzae type b

Ireland / HPRA · IRL · Sep 9, 2019

Key facts

Title VaccZyme™ Human Anti-Haemophilus Influenzae type b
Regulator Ireland / HPRA
Country IRL
Brand VaccZyme™ Human Anti-Haemophilus Influenzae type b
Manufacturer The Binding site
Models MK016, GLB124438, 1214569696, TSWS18, GLB125869, 413170, AE040, 435314
Event type Recall
Date Sep 9, 2019
Regulator page hpra.ie

At a glance

  • Yes 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

Browse all International device safety notices