International safety notice
Urgent Field Safety Notice for Arrow FiberOptix Intra-Aortic BalloonArrow Trerotola Over-The-Wire PTD Kit Percutane Catheter Kit by Arrow International Inc.
Germany / BfArM · DEU · Sep 23, 2021
Key facts
| Title | Urgent Field Safety Notice for Arrow FiberOptix Intra-Aortic BalloonArrow Trerotola Over-The-Wire PTD Kit Percutane Catheter Kit by Arrow International Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Arrow FiberOptix Intra-Aortic BalloonArrow Trerotola Over-The-Wire PTD Kit Percutane Catheter Kit |
| Manufacturer | Arrow International Inc. |
| Models | 13F20G0177, PT-12709-C, 13C20F0570, 13C20M0144, 14C21D0635, 13C20G0228, 13F20G0361, 13C20F0572, 14C20L0665, 13F20F0229, 13C21E1991, 13F20F0231 and 136 more |
| Date | Sep 23, 2021 |
| 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