Hollister 9786Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00610075167760), received between Jul 5, 2023 and Jan 15, 2025 — classified as 3 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJan 15, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT A HOLLISTER FEEDING TUBE ATTACHMENT DEVICE PEELED COMPLETELY AWAY FROM THE PATIENT'S SKIN DISLODGING THE NASOGASTRIC TUBE IT WAS SECURING. IT WAS REPORTED THAT THERE WAS NO INJURY BUT THE PATIENT REQUIRED A REINSERTION OF THE NG TUBE AND ADDITIONAL X-RAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21157448 ↗
• InjuryNov 14, 2023Improper or Incorrect Procedure or Method; Device Dislodged or Dislocated; Improper or Incorrect Procedure or Method; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE TAPE ON THE HOLLISTER FEEDING TUBE ATTACHMENT DEVICE DID NOT STAY SECURED TO THE PATIENT'S NOSE AND THE NASOGASTRIC TUBE WAS ABLE TO DISLODGE. IT WAS FURTHER REPORTED THAT THE TAPE ADHERED TO THE NOSE FOR LESS THAN 24 HOURS. THE ACCOUNT WENT ON TO REPORT THAT THIS IMPACTED THE PATIENT'S LENGTH OF STAY AS THEY REQUIRED ANOTHER PROCEDURE TO INSERT A TUBE. THEY ALSO REPORTED THAT THE TUBE IS A NASOJEJUNAL TUBE FOR FEEDING AND REQUIRED INSERTION UNDER SEDATION AND UNTIL REINSERTED, THEY WERE NOT MEETING THEIR NUTRITIONAL REQUIREMENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18129514 ↗
• InjuryJul 5, 2023Inadequate or Insufficient Training; Inadequate or Insufficient Training

  IT WAS REPORTED THAT A PATIENT WHO HAD A 12 FR FEEDING TUBE IN PLACE SECURED BY A HOLLISTER FEEDING TUBE ATTACHMENT DEVICE EXPERIENCED A TUBE DISLODGEMENT BECAUSE THE CLAMP DID NOT SECURELY HOLD THE TUBE IN PLACE AND THE TUBE WAS ABLE TO SLIDE THROUGH THE CLAMP. IT WAS REPORTED THAT THE DISLODGEMENT LED TO ASPIRATION LEADING TO RESPIRATORY DISTRESS, HYPOXIA, AND TACHYPNEA. IT WAS FURTHER REPORTED THAT CRACKLES WERE HEARD IN THE CHEST AND CONSOLIDATION IN LUNG WAS SEEN ON X-RAY. IT WAS REPORTED THAT THE PATIENT NEEDED REPEATED DEEP SUCTIONING, SEVERAL DAYS OF OXYGEN THERAPY, AND IV ANTIBIOTICS. THE ACCOUNT REPORTED THAT THE PATIENT RECOVERED FROM THE ASPIRATION EVENT BUT REMAINS IN THE HOSPITAL FOR OTHER REASONS. THE ACCOUNT REPORTED THAT THEY SWITCHED TO THE HOLLISTER TUBE ATTACHMENT DEVICE A COUPLE OF MONTHS AGO AND HAD NO EDUCATION OR TRAINING WHEN THIS SWITCH WAS MADE.

  Patient problems: Aspiration/Inhalation; Hypoxia

  MAUDE report 17255978 ↗