International safety notice

EHA343|EHA344|EHA346|EHA348|EHA353|EHA354|EHA356|EHA358|EHA443|EHA444|EHA446|EHA448|EHA453|EHA454|EHA456|EHA458|EHA463|EHA464|EHA466|EHA468|EHA473|EHA474|EHA476|EHA478|EHA553|EHA554|EHA556|EHA558|EHA563|EHA564|EHA566|EHA568

New Zealand / Medsafe Recalls · NZL · Dec 11, 2015

Key facts

Title EHA343|EHA344|EHA346|EHA348|EHA353|EHA354|EHA356|EHA358|EHA443|EHA444|EHA446|EHA448|EHA453|EHA454|EHA456|EHA458|EHA463|EHA464|EHA466|EHA468|EHA473|EHA474|EHA476|EHA478|EHA553|EHA554|EHA556|EHA558|EHA563|EHA564|EHA566|EHA568
Regulator New Zealand / Medsafe Recalls
Country NZL
Brand Biomet 3i Bellatek Encode Healing Abutment
Manufacturer Implant Innovations Inc
Models EHA463, EHA358, EHA568, EHA456, EHA556, EHA448, EHA466, EHA453, EHA478, EHA564, EHA554, EHA356 and 20 more
Event type Recall
Action type Recall
Date Dec 11, 2015
Regulator page medsafe.govt.nz

At a glance

  • Yes Recall
  • No Field safety notice
  • 10–99 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