International safety notice
Ανάκληση της παρτίδας 1005255170 του in vitro διαγνωστικού ιατροτεχνολογικού προϊόντος VIDAS High Sensitive Troponin I Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Mar 10, 2017
Key facts
| Title | Ανάκληση της παρτίδας 1005255170 του in vitro διαγνωστικού ιατροτεχνολογικού προϊόντος VIDAS High Sensitive Troponin I Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Models | 1005255170, 2132040435, 15562, 2106549500, 15232, Ν.1316, 02-03-2017, 17422, Ν.3730 |
| Event type | Recall, Safety Notice |
| Date | Mar 10, 2017 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 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