International safety notice
Urgent Field Safety Notice for ARES TM Antibiotic-Impregnated Catheter by Medtronic Inc
Germany / BfArM · DEU · Dec 14, 2020
Key facts
| Title | Urgent Field Safety Notice for ARES TM Antibiotic-Impregnated Catheter by Medtronic Inc |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ARES TM Antibiotic-Impregnated Catheter |
| Manufacturer | Medtronic Inc |
| Models | 0010336622, 0010265137, 0010289835, 0010384896, 0010369357, 0010369364, 0010052552, 0010297675, 95001, 0010384872, 0010384888, 0010289827 and 155 more |
| Date | Dec 14, 2020 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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