International safety notice

Ανάκληση της ακτινογραφικής διαφάνειας για γωνιακά εμφυτεύματα Certain Για να δείτε την απόφαση, πατήστε εδώ

Greece / EOF · GRC · Dec 11, 2015

Key facts

Title Ανάκληση της ακτινογραφικής διαφάνειας για γωνιακά εμφυτεύματα Certain Για να δείτε την απόφαση, πατήστε εδώ
Regulator Greece / EOF
Country GRC
Manufacturer BIOMET IMPLADEND 3i
Models Ν.1316, 87633, 130648, 85789, 03-12-2015, 6549500, 54642, 2040435
Event type Recall, Safety Notice
Date Dec 11, 2015
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes 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