Nutriline 1252.35GRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00849884000870), received between Jul 31, 2023 and Jul 31, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Leak/Splash” (1 report).

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

• MalfunctionJul 31, 2023Leak/Splash; Leak/Splash

  PICC NURSE WAS CALLED TO BEDSIDE OF PATIENT TO ASSESS WET DRESSING. PICC RN ASSESSED AND NOTED THAT PICC DRESSING WAS WET AND BIOPATCH WAS SOAKED. PICC RN LIFTED DRESSING AND NOTED THE PICC LEAKING IV FLUIDS AT THE HUB. PICC WAS REMOVED AND MD NOTIFIED. BEDSIDE NURSE REPORTED THAT DRESSING HAD BEEN CHANGED 2 HOURS PRIOR TO THE LINE LEAKING.

  Patient problems: Failure of Implant

  MAUDE report 17423681 ↗