BD Syringe NRFit™ Lok 400174Recalls & reported problems
Becton, Dickinson And Company · BD® 10mL Syringe NRFit™ Lok · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00382904001742), received between Sep 9, 2022 and Mar 4, 2025 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (12 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.
Reports received per month
Most reported problems
Device problems
- Device Markings/Labelling Problem12
- Defective Component3
- Volume Accuracy Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions13
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 4, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21519011 ↗MalfunctionJan 7, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21095639 ↗MalfunctionJan 2, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21063198 ↗MalfunctionDec 26, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE BD SYRINGE NRFIT¿ LOK HAD MIXED PRODUCT / LOTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WE HAVE HAD AN ISSUE DISCOVERED BY 2 SITES WHEN USING NRFIT SYRINGES AND DRAWING UP NEEDLE FOR SPINAL. THE SYRINGE WAS NOT COMPATIBLE WITH THE NEEDLE BUT COULD BE CONNECTED TO ORDINARY IV CANNULA. THIS IS AFFECTING BATCH (B)(4) WITH THE LOT NUMBER 1041220 CAN YOU PLEASE ADVISE DEAN AND I IF THE SUPPLIER WILL BE REPLACING OR CREDITING US FOR THE (B)(4) EA HE HAS MOVED INTO QUARANTINE LAST WEEK, AND WHAT WE NEED TO DO WITH THEIR QUARANTINED STOCK? ADDITIONAL INFORMATION PROVIDED: CUSTOMER RESPONSE RECEIVED INFORMATION REQUESTED IS BELOW; COMPANY: SPIRE HEALTHCARE NATIONAL DISTRIBUTION CENTRE COLLECTION POINT: GOODS IN/OUT STREET, NUMBER: (B)(6) BUILDING, FLOOR: NDC POSTAL CODE: (B)(6). COUNTRY: UK PLEASE ALSO PROVIDE US WITH THE PHONE NUMBER OF A PERSON WHO CAN BE CONTACTED BY THE CARRIER. CONTACT NAME: (B)(6). PHONE NUMBER: (B)(6) E-MAIL ADDRESS: [email protected].
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21023405 ↗MalfunctionDec 22, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20997689 ↗MalfunctionNov 18, 2024Volume Accuracy Problem; Volume Accuracy Problem
POST INVESTIGATION FINDINGS REVEALED THE ADDITIONAL FAILURE OF MIXED PRODUCT / LOTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20714280 ↗MalfunctionNov 12, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20668584 ↗MalfunctionNov 5, 2024Defective Component; Device Markings/Labelling Problem; Defective Component; Device Markings/Labelling Problem
NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20611934 ↗MalfunctionOct 22, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE BD SYRINGE NRFIT¿ LOK HAD MIXED PRODUCT / LOTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER TRANSLATED FROM SPANISH TO ENGLISH: 10 ML MEDICATION LOADING SYRINGE OF THE COMPANY BD, LABELED AS NRFIT LOK CONNECTION AND YELLOW COLOR IDENTIFYING THE MATERIAL FOR THE ADMINISTRATION OF PERINEURAL MEDICATION THAT NEVERTHELESS PRESENTS LUER LOK CONNECTION. THE INCIDENT DOES NOT REACH THE PATIENT BUT POSES A RISK OF CROSS-CONNECTION IN IV MEDICATION PORTS. IN OUR CENTER, ALL THE MATERIAL FOR PERINEURAL MEDICATION ADMINISTRATION HAS BEEN CHANGED TO NRFIT CONNECTIONS TO AVOID INTRAVENOUS CROSS-CONNECTION. THIS PROBLEM REPRESENTS A VIOLATION OF THE SAFETY BARRIER POSED BY THIS SET WITH THE RISK OF LETHAL INTRAVENOUS MEDICATION ADMINISTRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20510129 ↗MalfunctionOct 22, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE BD SYRINGE NRFIT¿ LOK HAD MIXED PRODUCT / LOTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: SYRINGES MARKED AND PACKAGED AS BEING NRFIT¿ BUT WITH THE LUER CONNECTOR!!! BEFORE USE SYRINGES MARKED AND PACKAGED AS BEING NRFIT¿ BUT WITH THE LUER CONNECTOR, PLEASE SEE ATTACHED PICTURE. THEY HAVE ASKED THEIR 3PL DISTRIBUTOR (ONEMED) TO STOP ALL OUTGOING DELIVERIES TO THE HOSPITALS. THE COMPLAINANT HAS ASKED FOR AN URGENT MEETING WITH ME TODAY TO DISCUSS THE COMPLAINT AND I WILL TRY TO GET AS MUCH INFORMATION AS POSSIBLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20510019 ↗MalfunctionMay 17, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THE BD SYRINGE NRFIT¿ LOK WITH MIXED PRODUCT/LOTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THIS LOTS OF REFERENCE ARE MIXED SYRINGES NRFIT WITH SYRINGES LUERLOCK, . ALL WITHIN THE SAME BOX WITH THE SAME REFERENCE (NRFIT) AND THE SAME ASSEMBLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19346824 ↗MalfunctionSep 28, 2022Defective Component; Device Markings/Labelling Problem; Defective Component; Device Markings/Labelling Problem
IT WAS REPORTED WHILE USING BD® 10ML SYRINGE NRFIT¿ LOK (STERILE) THE TIP OF THE LUER WAS DEFORMED. THIS OCCURRED TWICE. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ONE OF OUR TESTING SITES INITIALLY BELIEVED THE NRFIT SYRINGES TO BE INCOMPATIBLE WITH THE NRFIT NEEDLES; HOWEVER UPON CLOSER INSPECTION THEY CONFIRMED THE NRFIT SYRINGE CONTAINED A DEFECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15498951 ↗MalfunctionSep 9, 2022Defective Component; Device Markings/Labelling Problem; Defective Component; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE BD® PLASTIC NRFIT¿ SYRINGE WAS WITH OR WITHOUT LUERLOCK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER, TRANSLATED FROM DUTCH TO ENGLISH: WE HAVE FOUND THAT FOR ITEM NUMBER 400174 WITH LOT NUMBER 1041220, THERE ARE PRODUCTS WITH AND WITHOUT LUERLOCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15395696 ↗
Other Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact devices
- BD Syringe NRFit™ Slip 400051Becton, Dickinson And Company · Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact6 reports
- BD Syringe NRFit™ Lok 400182Becton, Dickinson And Company · Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact1 report
- BD Syringe NRFit™ Lok 400183Becton, Dickinson And Company · Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact1 report
- BD Syringe NRFit™ Lok 400173Becton, Dickinson And Company · Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact1 report
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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