AVANOS 46904Recalls & reported problems
Avanos Medical, Inc. · CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00350770469041), received between May 8, 2024 and May 8, 2024 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Aspiration/Inhalation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 8, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE PATIENT PULLED THEIR 16 FRENCH SUMP TUBE THROUGH A 16 FRENCH CORGRIP CLIP AND HAD AN ASPIRATION EVENT." THE REPORTER "FEELS THAT THE PRODUCT WORKS WELL AND THAT THE STAFF FAILED TO REPORT THE TUBE LENGTH AFTER EACH SHIFT. SHE FELT THAT THIS SHOULD HAVE BEEN CAUGHT BY THE STAFF AND HAS REQUESTED ADDITIONAL EDUCATION ON THE PRODUCT FOR THEIR TEAM.". THE PATIENT'S INITIAL DIAGNOSIS WAS SUBDURAL HEMATOMA, STROKE, AND DEMENTIA. THE SUMP TUBE WAS PLACED ON OR BEFORE THE (B)(6) AND THE ASPIRATION EVENT OCCURRED ON(B)(6). THE USER FACILITY NOTES TUBES ARE TYPICALLY PLACED AT 65CM AND THE TUBE WAS AT 23CM AT TIME OF ASPIRATION (WITH 16 FRENCH CORGRIP STILL ATTACHED). THE PATIENT IS CURRENTLY ON A VENTILATOR WITH A TRACHEOSTOMY TUBE AND A PERCUTANEOUS ENDOSCOPIC GASTROSTOMY (PEG). THE PATIENT IS RECEIVING CARE IN A LONG-TERM ACUTE CARE HOSPITALS (LTACHS). ADDITIONAL INFORMATION RECEIVED 29-APR-2024 STATING "PATIENT HAD BEEN INTUBATED ON ADMISSION BUT HAD BEEN EXTUBATED AND DOING WELL." FOLLOWING THIS EVENT THE PATIENT NEEDED IMMEDIATE RE-INTUBATION.
Patient problems: Aspiration/Inhalation
MAUDE report 19268076 ↗
Other Tubes, gastrointestinal (and accessories) devices
- Bard® DigniShield® Stool Management System SMS002C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 deaths525 reports
- CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)1 recall22 deaths134 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000720Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death170 reports
- EndoVive Safety PEG Kit M00566470Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 recall1 death111 reports
- Kangaroo 8884711253Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)152 reports
- NutraGlide Nasal Feeding Tube ENFT-05055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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