International safety notice

Ανάκληση παρτίδας σετ διαδερμικού εισαγωγέα θηκαριού Super Arrow-Flex Για να δείτε την απόφαση, πατήστε εδώ

Greece / EOF · GRC · Jan 5, 2011

Key facts

Title Ανάκληση παρτίδας σετ διαδερμικού εισαγωγέα θηκαριού Super Arrow-Flex Για να δείτε την απόφαση, πατήστε εδώ
Regulator Greece / EOF
Country GRC
Models 88032, Γ.Π.ΟΙΚ.130648, CF0014630, CL-07645, 23-12-2010, 1012177, 6507540, 6549500, 30-8-2009
Event type Recall, Safety Notice
Date Jan 5, 2011
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes Field safety notice

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