CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System 120008151Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00350770005997), received between Jun 9, 2026 and Jun 9, 2026 — classified as 2 injuries.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 9, 2026Adverse Event Without Identified Device or Use Problem

  AVANOS MEDICAL INC. RECEIVED A SINGLE REPORT THAT REFERENCED DIFFERENT INCIDENTS, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING DIFFERENT PATIENTS. THIS IS THE SECOND OF TWO REPORTS. REFER TO 3011270181-2026-00084 FOR THE FIRST REPORT. THE CUSTOMER REPORTED A PRESSURE INJURY ASSOCIATED WITH USE OF A TUBE RETENTION SYSTEM. ADDITIONAL INFORMATION RECEIVED ON MAY 20, 2026, REPORTED THAT THE RETENTION TETHER BECAME EMBEDDED IN THE PATIENT'S SKIN, WITH SKIN REPORTEDLY GROWING OVER THE TETHER. THE CONDITION WAS IDENTIFIED DURING REMOVAL OF THE FEEDING TUBE AND RETENTION SYSTEM ON (B)(6) 2026. THE DEVICE HAD REPORTEDLY BEEN PLACED AT ANOTHER FACILITY ON (B)(6) 2026. NO PATIENT DEMOGRAPHIC INFORMATION, MEDICAL INTERVENTION DETAILS, OR PATIENT OUTCOME INFORMATION WERE PROVIDED.

  Patient problems: Device Embedded In Tissue or Plaque; Pressure Sore/Ulcer

  MAUDE report 25448993 ↗
• InjuryJun 9, 2026Adverse Event Without Identified Device or Use Problem

  AVANOS MEDICAL INC. RECEIVED A SINGLE REPORT THAT REFERENCED DIFFERENT INCIDENTS, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING DIFFERENT PATIENTS. THIS IS THE FIRST OF TWO REPORTS. REFER TO 3011270181-2026-00085 FOR THE SECOND REPORT. THE CUSTOMER REPORTED A PRESSURE INJURY ASSOCIATED WITH USE OF A TUBE RETENTION SYSTEM. ADDITIONAL INFORMATION RECEIVED ON MAY 20, 2026, REPORTED THAT THE PRESSURE INJURY EXTENDED TO BONE AND WAS DESCRIBED AS SMALL IN AREA BUT DEEP. NO PATIENT DEMOGRAPHIC INFORMATION, MEDICAL INTERVENTION DETAILS, OR PATIENT OUTCOME INFORMATION WERE PROVIDED DESPITE FOLLOW-UP REQUESTS.

  Patient problems: Pressure Sore/Ulcer

  MAUDE report 25448992 ↗