BD Vacutainer Urinalysis Transfer Straw KitRecalls & reported problems across all models
Becton, Dickinson And Company · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 0
We found 2 models of BD Vacutainer Urinalysis Transfer Straw Kit by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 20 adverse event reports in the FDA's MAUDE database, received between Apr 12, 2022 and Aug 25, 2026 — classified as 20 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported BD Vacutainer Urinalysis Transfer Straw Kit problems
Device problems
- Fluid/Blood Leak11
- Product Quality Problem3
- Break1
- Component Missing1
- Loss of or Failure to Bond1
- Material Discolored1
- Separation Problem1
- Short Fill1
Patient problems
- No Clinical Signs, Symptoms or Conditions20
BD Vacutainer Urinalysis Transfer Straw Kit models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Vacutainer® Urinalysis Transfer Straw Kit 364990SYSTEM, TRANSPORT, AEROBIC11 reports
- BD Vacutainer® Urinalysis Transfer Straw Kit 364943SYSTEM, TRANSPORT, AEROBIC9 reports
Recent BD Vacutainer Urinalysis Transfer Straw Kit adverse event reports
The 15 most recent reports across all models, 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 ↗MalfunctionAug 13, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED BEFORE USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT THE CANNULA SEPARATED FROM THE STRAW ON TWO DEVICES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22797166 ↗MalfunctionMar 12, 2025Separation Problem; Separation Problem
IT WAS REPORTED THAT PRIOR TO USING BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT, THE STRAW OF AN UNSPECIFIED NUMBER OF DEVICES EITHER BREAKS OFF, BENDS, OR PULLS OUT WITH THE NEEDLE STILL ATTACHED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21584367 ↗MalfunctionOct 11, 2024Break; Break
IT WAS REPORTED BEFORE USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT ONE STRAW SEPARATED FROM THE HOLDER. ADDITIONALLY ONE KIT HAD A HALF A STRAW MISSING WHILE ANOTHER KIT HAD HALF A STRAW EXTRA. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20434306 ↗MalfunctionNov 9, 2023Component Missing; Component Missing
IT WAS REPORTED WHEN USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT CUSTOMER THEY ONLY RECEIVED THE STRAW BUT NOT THE CONICAL TUBE. NO PATIENT IMPACTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: CUSTOMER PROBLEM: CUSTOMER IS REPORTING THEY ONLY RECEIVED THE STRAW BUT NOT THE CONICAL TUBE. AFFECTED LOT NUMBER 3062535.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18100273 ↗
Other Becton, Dickinson And Company products
- BD Vacutainer SST10 models · 4,985 reports · 3 recalls
- BD Luer-Lok48 models · 5,117 reports
- BD Insyte Autoguard33 models · 4,465 reports · 8 recalls
- BD SafetyGlide17 models · 2,185 reports
- BD Vacutainer Eclipse Blood Collection Needle4 models · 1,880 reports
- BD Vacutainer Push Button Blood Collection Set9 models · 1,831 reports
- BD Nexiva25 models · 1,614 reports · 1 recall
- BD BACTEC MGIT Mycobacteria Growth Indicator Tubes2 models · 1,554 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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