International safety notice
Ανάκληση προϊόντος ACHILLON Suture System Για να δείτε την απόφαση, πατήστε εδώ
Greece / EOF · GRC · Jul 29, 2016
Key facts
| Title | Ανάκληση προϊόντος ACHILLON Suture System Για να δείτε την απόφαση, πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Manufacturer | στην Ελλάδα: ARTHROKINETICS E.E. |
| Models | Ν.1316, 130648, 27-6-2016, 6549500, 51357, 2040527 |
| Event type | Recall, Safety Notice |
| Date | Jul 29, 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