International safety notice
Teleflex Medical
United Kingdom / MHRA · GBR · Nov 1, 2022
Key facts
| Title | Teleflex Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | RUSCH Ureteral Catheters; RUSCH Superglide Integal Plus; RUSCH Valve Uretheral Stents; RUSCH Valve DD Uretheral Stents |
| Manufacturer | Teleflex Medical |
| Models | 71F21C0585, 71F18B0590, 71F19M0526, 71F21D0541, 71F20G0150, 71F18C1103, 71F19L1235, 264500-000050, 71F19H2794, 71F18F2827, 71F20H1319, 71F20F2221 and 1888 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Nov 1, 2022 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes 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