CORGRIP* SR NG/NI Tube Retention System 26-014Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00350770005638), received between Jul 10, 2024 and Aug 6, 2024 — 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.

• InjuryAug 6, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED, "¿WE GOT A NEW PLACEMENT WITH CORGRIP SR BUT THE PATIENT PULLED THE TUBE OUT. WE PUT IN A NEW TUBE APPROXIMATELY 45 MINUTES LATER, BUT FIVE MINUTES AFTER PLACING A NEW TUBE, A BIG BLEEDING STARTED FROM THE NOSE AND MOUTH AND THE OXYGEN SATURATION DROPPED MASSIVELY. THE PATIENT PULLED HIS TUBE / CORGRIP SR AND SINCE HE HAD A DELIRIUM, IT WASN¿T NOTICED THAT HE ALREADY HAD A BLEED. DUE TO THIS BLEEDING, THE PATIENT WAS INTUBATED, HAD A BRONCHOSCOPY AND A TAMPONADE. THE CONDITION OF THE PATIENT UNFORTUNATELY WORSENED SINCE THE BLOOD ALREADY HAD ENTERED THE LUNG." PER ADDITIONAL INFORMATION RECEIVED ON 17JUL2024, ¿PATIENT IS IMPROVING SLOWLY, BUT THEY HOPE TO EXTUBATE THE PATIENT LATER TODAY OR TOMORROW.¿ PER ADDITIONAL INFORMATION RECEIVED ON 18JUL2024, ¿PATIENT WAS EXTUBATED YESTERDAY AND IS DOING FINE.¿

  Patient problems: Hemorrhage/Blood Loss/Bleeding; Low Oxygen Saturation

  MAUDE report 19919975 ↗
• 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. PATIENT IS INTUBATED WITH A 14 FR NASOGASTRIC (NG) TUBE. KNOT IS STILL FIRMLY TIED. CLAMP HAS BEEN ROTATED FOR 90 DEGREES (AND CAN¿T BE TURNED BACK). A RED, SKINNED LESION ON THE LOWER SIDE OF THE COLUMELLA WHERE THE CORGRIP SR TETHER HAS CUT THROUGH THE SKIN. CORGRIP SR REMOVED AND NG TUBE IS FIXATED WITH NOSE PLASTER. THE DEVICE WAS IN USE FOR FOUR DAYS. NO SEVERE PATIENT HARM. PATIENT IS STILL IN INTENSIVE CARE UNIT (ICU) FOR INJURIES NOT RELATED TO THIS INCIDENT.

  Patient problems: Erythema; Localized Skin Lesion

  MAUDE report 19711537 ↗