International safety notice

Ανάκληση της παρτίδας N6L0351X του ιατροτεχνολογικού προϊόντος “Εndo GIATM Black Radial with Tri-StapleTM Technology” Για να δείτε την απόφαση πατήστε εδώ

Greece / EOF · GRC · Oct 10, 2017

Key facts

Title Ανάκληση της παρτίδας N6L0351X του ιατροτεχνολογικού προϊόντος “Εndo GIATM Black Radial with Tri-StapleTM Technology” Για να δείτε την απόφαση πατήστε εδώ
Regulator Greece / EOF
Country GRC
Brand Covidien LLC (USA)
Manufacturer Medtronic Hellas S.A
Models 81658, N6L0351X, 28-09-2017, 82414, 2040435, Ν.1316, 6549500, Ν6L0351X
Event type Recall, Safety Notice
Date Oct 10, 2017
Regulator page eof.gr

At a glance

  • Yes Recall
  • Yes Field safety notice
  • 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