BD Vacutainer Push Button Blood Collection SetRecalls & reported problems across all models
Becton, Dickinson And Company · 9 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,831
- Deaths reported
- 0
- Injuries reported
- 90
- Recalls
- 0
We found 9 models of BD Vacutainer Push Button Blood Collection Set by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 1,831 adverse event reports in the FDA's MAUDE database, received between Oct 20, 2017 and Sep 30, 2026 — classified as 90 injuries, 1,741 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (694 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 Push Button Blood Collection Set problems
Device problems
- Leak/Splash694
- Fluid/Blood Leak348
- Difficult or Delayed Activation165
- Product Quality Problem106
- Device Contamination with Chemical or Other Material63
- Short Fill53
- Break49
- Crack42
Patient problems
- No Clinical Signs, Symptoms or Conditions850
- No Known Impact Or Consequence To Patient650
- No Consequences Or Impact To Patient159
- Needle Stick/Puncture82
- No Patient Involvement36
- Exposure to Body Fluids31
- No Information25
- Blood Loss8
BD Vacutainer Push Button Blood Collection Set models
9 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Vacutainer® Push Button Blood Collection Set 367342Set, administration, intravascular781 reports
- BD Vacutainer® Push Button Blood Collection Set 367344Tubes, vials, systems, serum separators, blood collection464 reports
- BD Vacutainer® Push Button Blood Collection Set 367338Set, administration, intravascular194 reports
- BD Vacutainer® Push Button Blood Collection Set 367336Set, administration, intravascular152 reports
- BD Vacutainer® Push Button Blood Collection Set 367324Tubes, vials, systems, serum separators, blood collection133 reports
- BD Vacutainer® Push Button Blood Collection Set 367326Set, administration, intravascular51 reports
- BD Vacutainer® Push Button Blood Collection Set 367341Set, administration, intravascular36 reports
- BD Vacutainer® Push Button Blood Collection Set 367323Set, administration, intravascular15 reports
- BD Vacutainer® Push Button Blood Collection Set 367335Set, administration, intravascular5 reports
Recent BD Vacutainer 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, 2026Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954892 ↗MalfunctionSep 30, 2026Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954891 ↗MalfunctionSep 30, 2026Difficult or Delayed Activation
It was reported that after using the BD Vacutainer® Push Button Blood Collection Set, one (1) unit exhibited difficulty in retracting the needle. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946954 ↗MalfunctionSep 29, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936983 ↗MalfunctionSep 29, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50936973 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935966 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935052 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50935041 ↗MalfunctionSep 29, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933758 ↗MalfunctionSep 16, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50793764 ↗MalfunctionSep 15, 2026Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780205 ↗MalfunctionSep 15, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780203 ↗MalfunctionSep 14, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764379 ↗MalfunctionSep 14, 2026Fluid/Blood Leak; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50763171 ↗MalfunctionSep 14, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50761287 ↗
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 Nexiva25 models · 1,614 reports · 1 recall
- BD BACTEC MGIT Mycobacteria Growth Indicator Tubes2 models · 1,554 reports
- BD Vacutainer UltraTouch Push Button Blood Collection Set6 models · 1,468 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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