International safety notice
Percuvance® Percutaneous Shaft 29cm and Percuvance® Percutaneous Shaft 36cm
Ireland / HPRA · IRL · Feb 1, 2019
Key facts
| Title | Percuvance® Percutaneous Shaft 29cm and Percuvance® Percutaneous Shaft 36cm |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Percuvance® Percutaneous Shaft 29cm and Percuvance® Percutaneous Shaft 36cm |
| Manufacturer | Teleflex Medical |
| Models | 73H1700728, 73F1600086, 73F1700584, 73B1700180, 73J1700100, 73G1600207, 73A1700531, 73B1700523, 73M1600231, PCVSH3, 73C1600058, 73J1600394 and 29 more |
| Event type | Recall |
| Date | Feb 1, 2019 |
| Regulator page | hpra.ie |
At a glance
- Yes 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