AVANOS 95816Recalls & reported problems
Avanos Medical, Inc. · MIC* Standard PEG Kit - Push Method · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00350770958163), received between May 1, 2026 and May 1, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Complete Blockage” (1 report).
14 other recalls cover devices cleared under the same FDA submission (K924065); they may or may not involve this specific model.
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
- Complete Blockage1
- Entrapment of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 1, 2026Complete Blockage; Entrapment of Device
IT WAS REPORTED THAT A PATIENT HAD A PEG TUBE WITH BUMPER INSERTED 3 YEARS AGO. BACK THEN, THE PATIENT WAS DISCHARGED TO A NURSING HOME FOR LONG TERM CARE. HOWEVER, THE NURSING HOME WERE NOT AWARE THAT CORFLO PEG FIXATOR HAD TO BE OPENED, TUBE ADVANCED AND ROTATED WEEKLY TO PREVENT BURIED BUMPER SYNDROME. ON (B)(6) 2026 NURSING HOME STAFF WERE UNABLE TO FLUSH PEG. THE PATIENT WAS SENT TO THE HOSPITAL, AND THEY DISCOVERED THAT THE PATIENT HAD BURIED BUMPER SYNDROME. THE PATIENT UNDERWENT A SURGICAL PROCEDURE TO REMOVE BURIED BUMPER AND HAVE NEW STOMA SITE FORMED FOR NEW PEG. FORMAL TRAINING GIVEN TO NURSING HOME BY HOSPITAL DIETICIAN TO PREVENT ANY REOCCURRENCE OF BURIED BUMPER SYNDROME. THE PATIENT'S CONDITION IS STABLE, DISCHARGED FROM HOSPITAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25059077 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K924065. One submission often covers many models, so check the product and lot details in each record.
- Z-2349-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24
- Z-2342-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No
- Z-2346-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
- Z-2343-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No
- Z-2351-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
- Z-2352-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24
- Z-2341-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
- Z-2347-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Comp
- Z-2345-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
- Z-2348-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20
- Z-2350-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14
- Z-2344-2026 · Apr 30, 2026 · Open, ClassifiedProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14
- Z-0565-2022 · Dec 22, 2021 · TerminatedMIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL
- Z-0566-2022 · Dec 22, 2021 · TerminatedMIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL
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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