International safety notice
Ανάκληση παρτίδας 500300 των συρίγγων μιας χρήσης της εταιρείας NOVAPHARM Για να δείτε την απόφαση, πατήστε εδώ
Greece / EOF · GRC · Apr 7, 2015
Key facts
| Title | Ανάκληση παρτίδας 500300 των συρίγγων μιας χρήσης της εταιρείας NOVAPHARM Για να δείτε την απόφαση, πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | στην Ελλάδα: NOVAPHARM - ΒΛΑΝΤΗΣ Π ΑΛΕΞΙΟΥ Α ΟΕ |
| Models | 130648, 6549500, Ν.1316, ΒΕΝΙΖΈΛΟΥ26, 2040435, 21985, 500300, 2018-11 |
| Event type | Recall, Safety Notice |
| Date | Apr 7, 2015 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models 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