BD Vacutainer UltraTouch Push Button Blood Collection SetRecalls & reported problems across all models
Becton, Dickinson And Company · 6 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,468
- Deaths reported
- 0
- Injuries reported
- 55
- Recalls
- 0
We found 6 models of BD Vacutainer UltraTouch Push Button Blood Collection Set by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 1,468 adverse event reports in the FDA's MAUDE database, received between Oct 17, 2017 and Sep 30, 2026 — classified as 55 injuries, 1,413 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (456 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 UltraTouch Push Button Blood Collection Set problems
Device problems
- Leak/Splash456
- Fluid/Blood Leak343
- Difficult or Delayed Activation205
- Detachment of Device or Device Component98
- Product Quality Problem66
- Device Contamination with Chemical or Other Material53
- Short Fill45
- Volume Accuracy Problem40
Patient problems
- No Clinical Signs, Symptoms or Conditions1,015
- No Known Impact Or Consequence To Patient282
- No Consequences Or Impact To Patient64
- Needle Stick/Puncture50
- Exposure to Body Fluids30
- No Patient Involvement20
- No Information7
- Pain6
BD Vacutainer UltraTouch Push Button Blood Collection Set models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set 367364Set, administration, intravascular741 reports
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set 367365Set, administration, intravascular242 reports
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set 367392Set, administration, intravascular234 reports
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set 367393Set, administration, intravascular129 reports
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set 367363Set, administration, intravascular77 reports
- BD Vacutainer® UltraTouch™ Push Button Blood Collection Set 367391Set, administration, intravascular45 reports
Recent BD Vacutainer UltraTouch Push Button Blood Collection Set adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fluid/Blood Leak; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952583 ↗MalfunctionSep 30, 2026Activation Failure
It was reported while using BD Vacutainer® UltraTouch¿ Push Button Blood Collection Set, one (1) device had a retraction issue. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949378 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938986 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936975 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936968 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935960 ↗MalfunctionSep 28, 2026Fluid/Blood Leak; Difficult or Delayed Activation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923609 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922133 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922132 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922129 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922128 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50922112 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921285 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921280 ↗MalfunctionSep 28, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918131 ↗
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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