HalyardRecalls & reported problems across all models
Avanos Medical, Inc. · 232 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Halyard models — page 3
232 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Halyard 94831TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94843TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94850TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94851TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94872TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94873TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94884TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94906TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94917TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death1 report
- Halyard 94969TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 94993TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95458TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95475TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95481TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95484TUBE, GASTRO-ENTEROSTOMY1 report
- Halyard 95487TUBE, GASTRO-ENTEROSTOMY1 report
- Halyard 95493TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95636TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95638TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95646TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95649TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95656TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95659TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95660TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95667TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95674TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 95677TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 96898CATHETER AND TIP, SUCTION1 report
- Halyard 98693PROBE, RADIOFREQUENCY LESION1 report
- Halyard 98702TUBE, GASTRO-ENTEROSTOMY1 report
- Halyard 44066TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 report
- Halyard 79582Drape, surgical1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page