Teleflex Medical SDN. BHD.
FDA adverse event reports naming Teleflex Medical SDN. BHD. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: TELEFLEX MEDICAL SDN. BHD..
- Total reports
- 1,466
- Deaths
- 2
- Injuries
- 108
- Malfunctions
- 1,355
Reports per year
115
116
118
7019
20720
25221
27522
27123
14924
18625
5326
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Retention Type, BalloonEZL515
- Tube, Tracheal (W/Wo Connector)BTR338
- Condenser, Heat And Moisture (Artificial Nose)BYD119
- Airway, NasopharyngealBTQ118
- Catheter, UrologicalKOD93
- Filter, Bacterial, Breathing-CircuitCAH90
- Set, Tubing And Support, Ventilator (W Harness)BZO59
- Device, Fixation, Tracheal TubeCBH51
- Catheter, UrethralGBM36
- Tube, Bronchial (W/Wo Connector)BTS11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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