BD Syringe NRFit™ Slip 400051Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00382904000516), received between Sep 19, 2023 and Nov 24, 2024 — classified as 2 injuries, 4 malfunctions.

The most frequently reported specific device problem is “Defective Component” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 24, 2024Defective Component; Defective Component

  IT WAS REPORTED THAT THE BD SYRINGE 5ML S/T SSU NRFIT STOPPER WAS DEFECTIVE / DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: BEFORE USE, WHEN THEY TOOK THE SYRINGE OUT OF THE PACKAGE AND WERE ABOUT TO DRAW UP THE MEDICINE, THEY SAW THAT THE BLACK MEMBRANE LOOKED "MELTED" AND LAY AT AN ANGLED ANGLE INTO THE SYRINGE. THEY NEVER HAD TIME TO USE THE SYRINGE BUT SAW THE DEFECT BEFORE THE DRUG BEGAN TO BE WITHDRAWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20768678 ↗
• InjuryFeb 14, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: Bradycardia; Low Blood Pressure/ Hypotension

  MAUDE report 18705138 ↗
• InjuryFeb 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Urinary Retention

  MAUDE report 18678409 ↗
• MalfunctionNov 19, 2023Defective Component; Defective Component

  IT WAS REPORTED THAT THE BD SYRINGE NRFIT¿ SLIP STOPPER WAS DEFECTIVE/DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "WHEN THE NRFIT SYRINGE SLIP 5ML WAS OPENED, THE PLUNGER TIP SEEMS DAMAGED. THE NRFIT SYRINGE SLIP 5ML WAS NOT USED TO TREAT THE PATIENT."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18167094 ↗
• MalfunctionOct 11, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem

  NO ADDITIONAL INFORMATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17916849 ↗
• MalfunctionSep 19, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THE BD® PLASTIC NRFIT¿ SYRINGE HAD SCALE MARKING ISSUES. THE FOLLOWING WAS TRANSLATED FROM GERMAN TO ENGLISH: WHILE PERFORMING THE STUDY PROCEDURES THE PHYSICIAN NOTED THAT THE SCALE MARKING ON THE NRFIT SYRINGE COMES OFF AFTER HAVING BEEN TOUCHED A FEW TIMES. THE DEVICE STILL FULLFILLED ITS PURPOSE, THE USE WAS NOT AFFECTED IN ANY WAY, SINCE AT THE TIME THE SCALE WAS NOT READABLE ANY MORE THE SYRINGE HAD ALREADY FULFILLED ITS FUNCTION. THE CUSTOMER MERELY WANTED TO MENTION THAT THE MARKING IS NOT VERY DURABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17777142 ↗