International safety notice

Ανάκληση των παρτίδων Β10090, Β3697, B8766, B10089, B11666, B9355 του ιατροτεχνολογικού προϊόντος Humerus Integral Shaft and Stem implant component Για να δείτε την απόφαση πατήστε εδώ

Greece / EOF · GRC · Jan 26, 2017

Key facts

Title Ανάκληση των παρτίδων Β10090, Β3697, B8766, B10089, B11666, B9355 του ιατροτεχνολογικού προϊόντος Humerus Integral Shaft and Stem implant component Για να δείτε την απόφαση πατήστε εδώ
Regulator Greece / EOF
Country GRC
Models B10089, Β3697, Ν.3730, Ν.1316, Γ.Π.ΟΙΚ.130648, 30-8-2009, 14564, B9355, B8766, 2106549500, 2132040435, B11666 and 3 more
Event type Recall, Safety Notice
Date Jan 26, 2017
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes 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