International safety notice
Ανάκληση προϊόντος Trellis-8 Peripheral Infusion System Για να δείτε την απόφαση, πατήστε εδώ
Greece / EOF · GRC · Apr 7, 2015
Key facts
| Title | Ανάκληση προϊόντος Trellis-8 Peripheral Infusion System Για να δείτε την απόφαση, πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | Medtronic Hellas A.E. |
| Models | 30-8-2009, EVT808025, Γ.Π.ΟΙΚ.130648, EUT808030, EVT812015, 6549500, EVT812025, EUT812015, ΕVT808015, EUT812030, 2040527, TRELLIS-8 and 3 more |
| Event type | Recall, Safety Notice |
| Date | Apr 7, 2015 |
| 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