International safety notice
Ανάκληση μοντέλου 11859-36-05 του προϊόντος PLUM XLD W/Dataport Για να δείτε την απόφαση, πατήστε εδώ
Greece / EOF · GRC · Feb 23, 2016
Key facts
| Title | Ανάκληση μοντέλου 11859-36-05 του προϊόντος PLUM XLD W/Dataport Για να δείτε την απόφαση, πατήστε εδώ |
|---|---|
| Regulator | Greece / EOF |
| Country | GRC |
| Brand | Hospira Inc. (USA) |
| Manufacturer | AENORASIS S.A. |
| Models | 04-02-2016, AF141570, 11859-36-05, AD141603, LG152232, AD151535, Ν.1316, 6549500, MD151932, AE151545, 0574-0001, 0574-0007 and 13 more |
| Event type | Recall, Safety Notice |
| Date | Feb 23, 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