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Halyard 46905Recalls & reported problems

Avanos Medical, Inc. · HALYARD* CORGRIP* Nasogastric/Nasointestinal Feeding Tube Retention System · Class 2

All models of Halyard (232)

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 10680651469059), received between Jul 19, 2019 and Jul 19, 2019 — classified as 1 malfunction.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 19, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    AN MEDWATCH / FDA USER FACILITY REPORT # MW 2200710000-2019-8031 WAS RECEIVED AND THE FOLLOWING INFORMATION WAS PROVIDED: DESCRIBE EVENT: "THE PATIENT WAS BROUGHT TO MRI SCANNER IN THE RADIOLOGY/IMAGING DEPARTMENT TO HAVE A BRAIN SCAN. THE TECHNOLOGIST REPORTED THAT THE MAGNETIC WAND DID NOT INDICATE MAGNETISM NOTED NEAR THE PATIENT'S HEAD. THERE WERE ALSO NO VISIBLE SIGNS OF METAL DETECTED ON THE INSPECTION. IN THE MRI, THE STRING WITH THE MAGNET ATTACHED ON THE END PULLED SUGGESTING METAL PRESENT. UPON CLOSER INSPECTION OF THE CLOTH TAPE OF BRIDLE (NASOGASTRIC TUBE RETENTION SYSTEM), IT REVEALED THAT THE MAGNET TIP WAS STILL ON THE TAPE IMBEDDED IN CLOTH. THE SMALL MAGNET WAS REMOVED AND THE MRI WENT FORTH. ORIGINAL INTENDED PROCEDURE: THE SUGGESTION IS TO CUT OFF END TIP MAGNETS FROM ALL BRIDLES AFTER PLACEMENT PRIOR TO TAKING THE PATIENT TO MRI - TRAINING BEING OFFERED TO THE PROVIDER AND CLINICAL STAFF IN THE ICU BY THE CORGRIP REPRESENTATIVES DURING THE WEEK OF JUNE 16TH. ALSO, SECURE THE FEEDING TUBE A BRIDLE (NGT RETENTION SYSTEM) THAT MATCHES THE CORRECT SIZE OF THE FEEDING TUBE (EX FEEDING TUBE # 12, MATCHING BRIDLE = # 12 BRIDLE FOR SECURE ATTACHMENT). RESOURCE NURSE AND

    Patient problems: Foreign Body In Patient

    MAUDE report 8807649 ↗

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Sources and updates

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