BD Luer-Lok Female Cap 408531Recalls & reported problems
Becton, Dickinson And Company · CAP FEMALE LUER LOK S/SU · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382904085315), received between Oct 18, 2023 and Sep 5, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
- Contamination /Decontamination Problem1
- Device Contamination with Chemical or Other Material1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 5, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20144629 ↗MalfunctionAug 22, 2024Contamination; Contamination
NO ADDITIONAL INFORMATION
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20038961 ↗MalfunctionOct 18, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
MATERIAL#:408531; BATCH#: 2075464, 2159531. VERBATIM: COMPLAINT RECEIVED VIA EMAIL. EMAIL(S) ATTACHED. LOOSE PARTICLES AND DEBRIS WERE FOUND IN THE UNOPENED SYRINGE CAPS. DEBRIS WERE FOUND ON THE INNER PART OF UNOPENED SYRINGE CAPS, PARTICLES WERE EMBEDDED BETWEEN THE BACK AND PLASTIC BARRIERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17956729 ↗
Other CONTAINER, LIQUID MEDICATION, GRADUATED devices
- BD Luer Tip Caps 308341Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED1 recall3 reports
- BD Oral Syringe 305210Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED11 reports
- BD Oral Syringe 305209Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED6 reports
- BD Oral Syringe 305207Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED5 reports
- BD Oral Syringe 305220Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED4 reports
- BD Oral Syringe 305218Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED3 reports
- BD Syringe Tip Cap 305819Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED3 reports
- BD Oral Syringe 305219Becton, Dickinson And Company · CONTAINER, LIQUID MEDICATION, GRADUATED1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page