BD Syringe NRFit™ Lok 400183Recalls & reported problems
Becton, Dickinson And Company · BD® 50mL Syringe NRFit™ Lok · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382904001834), received between Dec 16, 2024 and Dec 16, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Leak/Splash1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 16, 2024Leak/Splash; Leak/Splash
ADDITIONAL INFORMATION RECEIVED . NO PATIENT IMPACT.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 20938563 ↗
Other Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact devices
- BD Syringe NRFit™ Lok 400174Becton, Dickinson And Company · Piston Syringe with neuraxial connector – epidural, peripheral, and/or indirect cerebral spinal fluid contact13 reports
- 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 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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