CORGRIP* SR NG/NI Tube Retention System 26-010Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00350770005614), received between Jul 10, 2024 and Mar 17, 2026 — classified as 2 injuries, 2 malfunctions.

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 17, 2026

  NEW BRIDLE IS LESS FLEXIBLE THAN PREVIOUS BRAND, STRINGS TO TIE IN A KNOT ARE WORSE QUALITY AND DO NOT STAY TIED, POSING A RISK FOR DISLODGMENT. OVERALL SEEMS WORSE QUALITY AND HARDER TO INSERT AND UTILIZE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24616674 ↗
• MalfunctionMar 13, 2026

  THE RETENTION SYSTEM HAS 2 STYLETS (YELLOW & WHITE), EACH WITH MAGNETS AT THE TIP. MAGNET FROM YELLOW STYLET CAME OFF AS IT WS BEING PULLED FROM PATIENT. MAGNET COULD HAVE FALLEN INSIDE NOSTRIL & TRAVEL INTO THE LUNGS, IT WASN'T SUPPOSED TO COME OFF FROM YELLOW STYLET. NORMALLY, MAGNET FROM WHITE TYLET WILL COME OFF & ATTACH TO YELLOW STYLET.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24589343 ↗
• InjuryJul 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED, CORGRIP SR PLACED ON THE (B)(6) 2024. KNOT BELOW CORGRIP SR IS COMPLETELY LOOSE. INSPECTION OF THE NOSTRIL AND SEE A LITTLE PRESSURE WOUND RIGHT BELOW THE COLUMELLA WHERE THE POINT OF THE CLAMP HAS PRESSED AGAINST THE NOSE. FURTHERMORE, A DEEPER, SKINNED LESION BELOW ON THE LOWER SIDE OF THE COLUMELLA WHERE THE CORGRIP SR TETHER HAS CUT THROUGH THE SKIN. CORGRIP SR HAS BEEN REMOVED AND NASOGASTRIC (NG) TUBE IS FIXATED WITH NOSE PLASTER. DEVICE WAS IN USE FOR FOUR DAYS. NO SEVERE PATIENT HARM. PATIENT IS STILL IN ICU FOR INJURIES NOT RELATED TO THIS INCIDENT.

  Patient problems: Localized Skin Lesion

  MAUDE report 19712387 ↗
• InjuryJul 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED, CORGRIP CAUSED BLEEDING AND PAIN. DEVICE WAS REMOVED A DAY LATER. NO SERIOUS INJURY OR MEDICAL INTERVENTIONS REPORTED. PER ADDITIONAL INFORMATION RECEIVED ON 21JUN2024, THE PATIENT WAS REPORTED TO BE ¿GOOD.¿ THE DEVICE WAS PLACED ON (B)(6) 2024 AND WAS REMOVED ON (B)(6) 2024.

  Patient problems: Hemorrhage/Blood Loss/Bleeding; Pain

  MAUDE report 19711560 ↗