NeoMed Enteral Feeding Tube PFTM8.0P-EORecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00817584012837), received between Apr 15, 2019 and Apr 15, 2019 — 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.

• InjuryApr 15, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  GASTRIC PERFORATION WAS IDENTIFIED IN A SEXTUPLET NICU PATIENT (PATIENT IDENTIFIER: (B)(6)) AFTER SIGNS AND SYMPTOMS OF ABDOMINAL DISTENTION. GASTRIC PERFORATION WAS IDENTIFIED AND CORRECTED IN SURGERY.

  Patient problems: Bowel Perforation

  MAUDE report 8514522 ↗
• InjuryApr 15, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  GASTRIC PERFORATION WAS IDENTIFIED IN A SEXTUPLET NICU PATIENT (PATIENT IDENTIFIER: (B)(6)) AFTER SIGNS AND SYMPTOMS OF ABDOMINAL DISTENTION. GASTRIC PERFORATION WAS IDENTIFIED AND CORRECTED IN SURGERY.

  Patient problems: Bowel Perforation

  MAUDE report 8514521 ↗