International safety notice
Ανάκληση παρτίδων του διαγνωστικού κιτ Alere TESTPACK + Plus STREP A Για να δείτε την απόφαση, πατήστε εδώ
Greece / EOF · GRC · Jun 16, 2016
Key facts
| Title | Ανάκληση παρτίδων του διαγνωστικού κιτ Alere TESTPACK + Plus STREP A Για να δείτε την απόφαση, πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | στην Ελλάδα: ΜΑΓΕΙΡΑΣ ΔΙΑΓΝΩΣΤΙΚΑ Α.Ε. |
| Models | 58334Κ100, 2040527, 59588Κ100, 45866, 59703Κ100, 57082Κ100, 56356Κ100, 58322Κ100, 56557Κ100, 57946Κ100, 59925Κ100, 6549500 and 20 more |
| Event type | Recall, Safety Notice |
| Date | Jun 16, 2016 |
| 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