International safety notice
Teleflex Medical
United Kingdom / MHRA · GBR · Jan 30, 2020
Key facts
| Title | Teleflex Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Arrow® EPIDURAL CATHETERIZATION Kits and Sets |
| Manufacturer | Teleflex Medical |
| Models | 71F19G1135, 13F19K0137, 23F19H0048, 71F19F1432, 71F19J1251, 23F19J0208, 71F19J0072, 13F19B0340, YC-02220, AA-05400-E, 71F19J1235, 71F19K2852 and 485 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Jan 30, 2020 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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