BD Vacutainer® Urinalysis Transfer Straw Kit 364990Recalls & reported problems
Becton, Dickinson And Company · KIT URIN TRANSTR 16X100 10.0 UA YEL · Class 1
All models of BD Vacutainer Urinalysis Transfer Straw Kit (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 30382903649908), received between Aug 18, 2026 and Aug 25, 2026 — classified as 11 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (11 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
- Fluid/Blood Leak11
Patient problems
- No Clinical Signs, Symptoms or Conditions11
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 25, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437740 ↗MalfunctionAug 25, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437735 ↗MalfunctionAug 25, 2026Fluid/Blood Leak
Report 5 of 7. It was reported that when using the BD Vacutainer® Urinalysis Transfer Straw Kit, an unspecified number of units broke while in the centrifuge, requiring recollection. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437734 ↗MalfunctionAug 25, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437733 ↗MalfunctionAug 25, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437728 ↗MalfunctionAug 25, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437727 ↗MalfunctionAug 25, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50437724 ↗MalfunctionAug 18, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50303788 ↗MalfunctionAug 18, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50303787 ↗MalfunctionAug 18, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50303786 ↗MalfunctionAug 18, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50303781 ↗
Other SYSTEM, TRANSPORT, AEROBIC devices
- BD Vacutainer® Urine Complete Cup Kit 364957Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC1 recall5 reports
- BBL™ CultureSwab™ EZ 220144Copan Italia SPA · System, Transport, Aerobic1 recall0 reports
- BD Vacutainer® Urine Transfer Straw 364966Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC22 reports
- BD Vacutainer® Urinalysis Cup Kit 364946Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC11 reports
- BD Vacutainer® Urine Collection Cups 364975Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC10 reports
- BD Vacutainer® Urinalysis Transfer Straw Kit 364943Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC9 reports
- BD Vacutainer® Urinalysis Cup Kit 364981Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC5 reports
- BD Vacutainer® Urinalysis Cup Kit 364989Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC3 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.
How reports and recalls are matched · Editorial policy · Report an error on this page