AVANOS 94831Recalls & reported problems
Avanos Medical, Inc. · MIC-KEY* G Feeding Tube-12-3-1.7 · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00350770948317), received between Dec 28, 2019 and Dec 28, 2019 — classified as 5 injuries.
The most frequently reported specific device problem is “Pressure Problem” (5 reports).
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Pressure Problem5
Patient problems
- Cellulitis5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryDec 28, 2019Pressure Problem; Pressure Problem
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED FIVE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING FIVE DIFFERENT EVENTS. THIS IS THE FOURTH OF FIVE REPORTS. REFER TO 9611594-2019-00269 FOR THE FIRST EVENT. REFER TO 9611594-2019-00270 FOR THE SECOND EVENT. REFER TO 9611594-2019-00271 FOR THE THIRD EVENT. REFER TO 9611594-2019-00273 FOR THE FIFTH EVENT. IT WAS REPORTED THE PATIENT EXPERIENCED SKIN BREAKDOWN AND PRESSURE UNDER THE NEWLY PLACED MIC-KEY GASTROSTOMY TUBE. THE SURGEONS PLACING THE DEVICE ARE DISAGREEING WITH THE WOUND OSTOMY TEAM THAT THESE ARE PRESSURE RELATED INJURIES. HOWEVER, THE WOUND OSTOMY CARE NURSE (WOCN) TEAM IS STAGING IT AS A PRESSURE INJURY (CELLULITIS).
Patient problems: Cellulitis
MAUDE report 9528456 ↗InjuryDec 28, 2019Pressure Problem; Pressure Problem
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED FIVE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING FIVE DIFFERENT EVENTS. THIS IS THE FIFTH OF FIVE REPORTS. REFER TO 9611594-2019-00269 FOR THE FIRST EVENT. REFER TO 9611594-2019-00270 FOR THE SECOND EVENT. REFER TO 9611594-2019-00271 FOR THE THIRD EVENT. REFER TO 9611594-2019-00272 FOR THE FOURTH EVENT. IT WAS REPORTED THE PATIENT EXPERIENCED SKIN BREAKDOWN AND PRESSURE UNDER THE NEWLY PLACED MIC-KEY GASTROSTOMY TUBE. THE SURGEONS PLACING THE DEVICE ARE DISAGREEING WITH THE WOUND OSTOMY TEAM THAT THESE ARE PRESSURE RELATED INJURIES. HOWEVER, THE WOUND OSTOMY CARE NURSE (WOCN) TEAM IS STAGING IT AS A PRESSURE INJURY (CELLULITIS).
Patient problems: Cellulitis
MAUDE report 9528454 ↗InjuryDec 28, 2019Pressure Problem; Pressure Problem
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED FIVE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING FIVE DIFFERENT EVENTS. THIS IS THE SECOND OF FIVE REPORTS. REFER TO 9611594-2019-00269 FOR THE FIRST EVENT. REFER TO 9611594-2019-00271 FOR THE THIRD EVENT. REFER TO 9611594-2019-00272 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00273 FOR THE FIFTH EVENT. IT WAS REPORTED THE PATIENT EXPERIENCED SKIN BREAKDOWN AND PRESSURE UNDER THE NEWLY PLACED MIC-KEY GASTROSTOMY TUBE. THE SURGEONS PLACING THE DEVICE ARE DISAGREEING WITH THE WOUND OSTOMY TEAM THAT THESE ARE PRESSURE RELATED INJURIES. HOWEVER, THE WOUND OSTOMY CARE NURSE (WOCN) TEAM IS STAGING IT AS A PRESSURE INJURY (CELLULITIS).
Patient problems: Cellulitis
MAUDE report 9528453 ↗InjuryDec 28, 2019Pressure Problem; Pressure Problem
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED FIVE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING FIVE DIFFERENT EVENTS. THIS IS THE THIRD OF FIVE REPORTS. REFER TO 9611594-2019-00269 FOR THE FIRST EVENT. REFER TO 9611594-2019-00270 FOR THE SECOND EVENT. REFER TO 9611594-2019-00272 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00273 FOR THE FIFTH EVENT. IT WAS REPORTED THE PATIENT EXPERIENCED SKIN BREAKDOWN AND PRESSURE UNDER THE NEWLY PLACED MIC-KEY GASTROSTOMY TUBE. THE SURGEONS PLACING THE DEVICE ARE DISAGREEING WITH THE WOUND OSTOMY TEAM THAT THESE ARE PRESSURE RELATED INJURIES. HOWEVER, THE WOUND OSTOMY CARE NURSE (WOCN) TEAM IS STAGING IT AS A PRESSURE INJURY (CELLULITIS).
Patient problems: Cellulitis
MAUDE report 9528452 ↗InjuryDec 28, 2019Pressure Problem; Pressure Problem
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED FIVE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING FIVE DIFFERENT EVENTS. THIS IS THE FIRST OF FIVE REPORTS. REFER TO 9611594-2019-00270 FOR THE SECOND EVENT. REFER TO 9611594-2019-00271 FOR THE THIRD EVENT. REFER TO 9611594-2019-00272 FOR THE FOURTH EVENT. REFER TO 9611594-2019-00273 FOR THE FIFTH EVENT. IT WAS REPORTED THE PATIENT EXPERIENCED SKIN BREAKDOWN AND PRESSURE UNDER THE NEWLY PLACED MIC-KEY GASTROSTOMY TUBE. THE SURGEONS PLACING THE DEVICE ARE DISAGREEING WITH THE WOUND OSTOMY TEAM THAT THESE ARE PRESSURE RELATED INJURIES. HOWEVER, THE WOUND OSTOMY CARE NURSE (WOCN) TEAM IS STAGING IT AS A PRESSURE INJURY (CELLULITIS).
Patient problems: Cellulitis
MAUDE report 9528450 ↗
Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices
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- 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
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 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
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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