PU Feeding Tube PFTM5.0P-EORecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00350770002330), received between Oct 3, 2023 and Oct 3, 2023 — classified as 3 injuries.

The most frequently reported specific device problem is “Malposition of Device” (3 reports).

1 other recall cover devices cleared under the same FDA submission (K082238); they may or may not involve this specific model.

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

• InjuryOct 3, 2023Malposition of Device; Malposition of Device

  AVANOS MEDICAL RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT EVENTS. THIS IS THE THIRD OF THREE REPORTS. REFER TO 3011270181-2023-00121 FOR THE FIRST EVENT. REFER TO 3011270181-2023-00122 FOR THE SECOND EVENT. IT WAS REPORTED PATIENT HAD A NASOGASTRIC TUBE PERFORATION WHILE IN THE NICU [NEONATAL INTENSIVE CARE UNIT]. THERE WAS NO REPORTED INJURY.

  Patient problems: Perforation

  MAUDE report 17865632 ↗
• InjuryOct 3, 2023Malposition of Device; Malposition of Device

  AVANOS MEDICAL RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT EVENTS. THIS IS THE SECOND OF THREE REPORTS. REFER TO 3011270181-2023-00121 FOR THE FIRST EVENT. REFER TO 3011270181-2023-00123 FOR THE THIRD EVENT. IT WAS REPORTED PATIENT HAD A NASOGASTRIC TUBE PERFORATION WHILE IN THE NICU [NEONATAL INTENSIVE CARE UNIT]. THERE WAS NO REPORTED INJURY.

  Patient problems: Perforation

  MAUDE report 17865613 ↗
• InjuryOct 3, 2023Malposition of Device; Malposition of Device

  AVANOS MEDICAL RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT EVENTS. THIS IS THE FIRST OF THREE REPORTS. REFER TO 3011270181-2023-00122 FOR THE SECOND EVENT. REFER TO 3011270181-2023-00123 FOR THE THIRD EVENT. IT WAS REPORTED PATIENT HAD A NASOGASTRIC TUBE PERFORATION WHILE IN THE NICU [NEONATAL INTENSIVE CARE UNIT]. THERE WAS NO REPORTED INJURY.

  Patient problems: Perforation

  MAUDE report 17865612 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K082238. One submission often covers many models, so check the product and lot details in each record.

• Z-0093-2019 · Jun 4, 2018 · Terminated
  NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm, 60cm, 90cm. The product consists of a polyurethane feeding tu