HUDSON RCIRecalls & reported problems across all models
Teleflex Incorporated · 152 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
HUDSON RCI models — page 2
152 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- HUDSON RCI IPN044763Tube, tracheal (w/wo connector)1 death1 report
- HUDSON RCI IPN044765Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044785Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044792Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044798Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044801Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044854TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 report
- HUDSON RCI IPN044898Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044899Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN044901Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN042605CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)1 report
- HUDSON RCI IPN044066CANNULA, NASAL, OXYGEN1 report
- HUDSON RCI IPN044067CANNULA, NASAL, OXYGEN1 report
- HUDSON RCI IPN046955CANNULA, NASAL, OXYGEN1 report
- HUDSON RCI IPN040618NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN048867Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN048869Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN048878Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN048891Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN048949Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN048958Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN048944Tube, tracheal (w/wo connector)1 report
- HUDSON RCI IPN049730CANNULA, NASAL, OXYGEN1 report
- HUDSON RCI IPN049142SPIROMETER, THERAPEUTIC (INCENTIVE)1 report
- HUDSON RCI IPN049292NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN049299NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN049108HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN049251NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN049309DEVICE, FIXATION, TRACHEAL TUBE1 report
- HUDSON RCI IPN049319SPIROMETER, THERAPEUTIC (INCENTIVE)1 report
- HUDSON RCI IPN049869BAG, RESERVOIR1 report
- HUDSON RCI IPN049797NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN049856AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 report
- HUDSON RCI IPN913881MASK, OXYGEN1 report
- HUDSON RCI IPN913908CANNULA, NASAL, OXYGEN1 report
- HUDSON RCI IPN914295ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE1 report
- HUDSON RCI IPN029718CONNECTOR, AIRWAY (EXTENSION)1 report
- 1 report
- HUDSON RCI IPN913797SET, TUBING AND SUPPORT, VENTILATOR (W HARNESS)1 report
- HUDSON RCI IPN913838Humidifier nebulizer kit1 report
- HUDSON RCI IPN913851Humidifier nebulizer kit1 report
- HUDSON RCI IPN913853Humidifier nebulizer kit1 report
- HUDSON RCI IPN913837Humidifier nebulizer kit1 report
- HUDSON RCI IPN049841HEATER, BREATHING SYSTEM W/WO CONTROLLER (NOT HUMIDIFIER OR NEBULIZER1 report
- HUDSON RCI IPN049826NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)1 report
- HUDSON RCI IPN049831NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN039348Ventilator, emergency, manual (resuscitator)1 report
- HUDSON RCI IPN914789NEBULIZER (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN916671CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)1 report
- HUDSON RCI IPN916677Nebulizer (direct patient interface)1 report
- HUDSON RCI IPN927526HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI 5-16137TUBE, TRACHEAL/BRONCHIAL, DIFFERENTIAL VENTILATION (W/WO CONNECTOR)1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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