International safety notice
Teleflex Medical
United Kingdom / MHRA · GBR · May 21, 2020
Key facts
| Title | Teleflex Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Arrow AutoCAT Intra-Aortic Balloon Pump (IABP) Series, AC3™ Series IABP System |
| Manufacturer | Teleflex Medical |
| Models | 181041F, 160919W, 180308W, 200324V, 160101V, 160112V, 150409V, 171011F, 200308F, 170302W, 150202W, 170950W and 663 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | May 21, 2020 |
| Regulator page | gov.uk |
At a glance
- No 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