International safety notice
Urgent corrective action for Source Administration Sets (SAS) used with Medrad Intego PET Infusion System, Bayer Medical Care / Bayer HealthCare
Germany / BfArM · DEU · Feb 3, 2016
Key facts
| Title | Urgent corrective action for Source Administration Sets (SAS) used with Medrad Intego PET Infusion System, Bayer Medical Care / Bayer HealthCare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Source Administration Sets (SAS) used with Medrad Intego PET Infusion System, Bayer Medical Care / Bayer HealthCare |
| Manufacturer | Urgent corrective action for Source Administration Sets (SAS) used with Medrad Intego PET Infusion System, Bayer Medical Care / Bayer HealthCare |
| Models | 50888287, 50871131, 50860994, 50888373, 1-800-633-7231, 50886467, 60000322, 50856405, 50878232, 50867921, 50881506, 50881394 and 37 more |
| Date | Feb 3, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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