International safety notice
Ανάκληση της παρτίδας N6L0351X του ιατροτεχνολογικού προϊόντος “Εndo GIATM Black Radial with Tri-StapleTM Technology” - ΟΡΘΗ ΕΠΑΝΑΛΗΨΗ Για να δείτε την απόφαση πατήστε εδώ
Greece / EOF · GRC · Nov 22, 2017
Key facts
| Title | Ανάκληση της παρτίδας N6L0351X του ιατροτεχνολογικού προϊόντος “Εndo GIATM Black Radial with Tri-StapleTM Technology” - ΟΡΘΗ ΕΠΑΝΑΛΗΨΗ Για να δείτε την απόφαση πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Brand | Covidien LLC (USA) |
| Manufacturer | AN. ΜΑΥΡΟΓΕΝΗΣ Α.Ε. |
| Models | 28-09-2017, 15-11-2017, 2040435, 6549500, N6L0351X, Ν6L0351X, 81658, 82414, Ν.1316 |
| Event type | Recall, Safety Notice |
| Date | Nov 22, 2017 |
| Regulator page | eof.gr |
At a glance
- Yes Recall
- Yes Field safety notice
- 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