BD Blunt Filter NRFit 400066Recalls & reported problems
Becton, Dickinson And Company · BD® Blunt Filter NRFit™ Needle, 18G x 1 1/2 in · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00382904000660), received between Feb 6, 2024 and Mar 5, 2026 — classified as 4 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
- Connection Problem1
- Defective Component1
- Labelling, Instructions for Use or Training Problem1
Patient problems
- Bradycardia2
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
- Low Blood Pressure/ Hypotension1
- Nausea1
- Urinary Retention1
- Vomiting1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 5, 2026Labelling, Instructions for Use or Training Problem
EVENT DATE VERIFIED WITH CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24519870 ↗MalfunctionOct 23, 2025Connection Problem; Connection Problem
MalfunctionSep 30, 2024Defective Component; Defective Component
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20334325 ↗InjuryMar 14, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE ABOVE MENTIONED CUSTOMER IS PARTICIPATING IN THE MDS-21NRFIT001 STUDY. THE PATIENT HAS COLLAPSED SECONDS AFTER THE BEGINNING OF THE STUDY PROCEDURE (SPINAL ANESTHESIA), DROP IN BLOOD PRESSURE AND BRADYCARDIA. THE ADVERSE EVENT RESOLVED STARTED ON 09-FEB-2024 AND RESOLVED ON THE SAME DATE. THE PATIENT EXPLAINED PREVIOUS COLLAPSE DURING PROSTATE BIOPSY DUE TO STRESS AND FEAR. THE SPINAL NRFIT NEEDLE WAS NOT SUCCESSFULLY PLACED DUE TO THE CIRCULATORY COLLAPSE OF THE PATIENT. ACTION TAKEN DUE TO THE ADVERSE EVENT: DEVICE REMOVED. RELATIONSHIP TO BD NRFIT SPINAL NEEDLE QUINCKE SET CATALOG NUMBER 400226, LOT NUMBER 2103704: NOT RELATED. RELATIONSHIP TO BD NRFIT SYRINGE SLIP 5ML CATALOG NUMBER 400051, LOT NUMBER 3117599: NOT RELATED . RELATIONSHIP TO BD NRFIT INTRODUCER AS PART OF THE SET CATALOG NUMBER 400226, LOT NUMBER 2103704: NOT RELATED. RELATIONSHIP TO BD NRFIT BLUNT FILTER CATALOG NUMBER 400066, LOT NUMBER 2327051: NOT RELATED. RELATIONSHIP TO PROCEDURE: CAUSAL.
Patient problems: Bradycardia
MAUDE report 18903080 ↗InjuryFeb 14, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADVERSE EVENT WITH NO MALFUNCTION, DEVICE UNRELATED. ADVERSE EVENT RELATED TO PROCEDURE ONLY.
Patient problems: Bradycardia; Low Blood Pressure/ Hypotension
MAUDE report 18704492 ↗InjuryFeb 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryFeb 6, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADVERSE EVENT WITH NO MALFUNCTION, DEVICE UNRELATED. ADVERSE EVENT RELATED TO PROCEDURE ONLY.
Patient problems: Nausea; Vomiting
MAUDE report 18655497 ↗
Other NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE devices
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- N/A 305200Becton, Dickinson And Company · NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE99 reports
- PneumoDart TM-317TyTek Medical Inc. · Needle, Aspiration And Injection, Disposable1 recall1 report
- TPAK TM-303TyTek Medical Inc. · Needle, Aspiration And Injection, Disposable1 recall0 reports
- N/A 305181Becton, Dickinson And Company · NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE32 reports
- SOL-M™ Blunt Fill Needle with 5 Micron Filter 110022Sol-Millennium Medical, Inc. · Needle, Aspiration And Injection, Disposable17 reports
- CONFIDENCE SPINAL CEMENT SYSTEM 283903611Medos International Sàrl · NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE17 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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