International safety notice

Ανάκληση παρτίδων του ιατροτεχνολογικού προϊόντος “Multirate Infusor” Για να δείτε την απόφαση πατήστε εδώ

Greece / EOF · GRC · Jul 10, 2017

Key facts

Title Ανάκληση παρτίδων του ιατροτεχνολογικού προϊόντος “Multirate Infusor” Για να δείτε την απόφαση πατήστε εδώ
Regulator Greece / EOF
Country GRC
Brand Βaxter Healthcare (Swisse) Έχοντας υπόψη
Manufacturer Baxter Hellas
Models 2C1154KP, 2C1155KP, 2040435, 6549500, 16Η040, 55426, 16K047, 16-06-2017, Ν.1316
Event type Recall, Safety Notice
Date Jul 10, 2017
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