RUSCHRecalls & reported problems across all models
Teleflex Incorporated · 220 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
RUSCH models — page 3
220 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- RUSCH IPN050513CATHETER, UROLOGICAL1 report
- RUSCH IPN050519CATHETER, UROLOGICAL1 report
- RUSCH IPN050424CATHETER, UROLOGICAL1 report
- RUSCH IPN040962Tube, tracheal (w/wo connector)1 report
- RUSCH IPN040964Tube, tracheal (w/wo connector)1 report
- RUSCH IPN041699TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 report
- RUSCH IPN041703TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 report
- RUSCH IPN041720TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 report
- RUSCH IPN054275CATHETER, RETENTION TYPE, BALLOON1 report
- RUSCH IPN045176LARYNGOSCOPE, RIGID1 report
- RUSCH IPN048415LARYNGOSCOPE, RIGID1 report
- RUSCH IPN048418LARYNGOSCOPE, RIGID1 report
- RUSCH IPN049328LARYNGOSCOPE, RIGID1 report
- RUSCH IPN049334LARYNGOSCOPE, RIGID1 report
- RUSCH IPN049954LARYNGOSCOPE, RIGID1 report
- RUSCH IPN915471LARYNGOSCOPE, RIGID1 report
- RUSCH IPN915474LARYNGOSCOPE, RIGID1 report
- RUSCH IPN915496LARYNGOSCOPE, RIGID1 report
- RUSCH IPN915573LARYNGOSCOPE, RIGID1 report
- RUSCH 220400140CATHETER, URETHRAL1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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