International safety notice
Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, Vascular Probe Intravascular Probe, Ma Recette Mitonnee Leg MP 6
Ireland / HPRA · IRL · Jan 3, 2024
Key facts
| Title | Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, Vascular Probe Intravascular Probe, Ma Recette Mitonnee Leg MP 6 |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, Vascular Probe Intravascular Probe, Ma Recette Mitonnee Leg MP 6 |
| Manufacturer | SYNOVIS LIFE TECHNOLOGIES INC. |
| Models | 50225, 60250BIOS, 50350, FA-2024-007, 50100, 60300, 60275, FT12300, 60175, 50125, 50275, 8-DEC-21 and 22 more |
| Event type | Safety Notice |
| Date | Jan 3, 2024 |
| Regulator page | hpra.ie |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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