BD Vacutainer SerumRecalls & reported problems across all models
Becton, Dickinson And Company · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 599
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 0
We found 5 models of BD Vacutainer Serum by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 599 adverse event reports in the FDA's MAUDE database, received between Nov 27, 2017 and Sep 30, 2026 — classified as 2 injuries, 597 malfunctions.
The most frequently reported specific device problem is “Short Fill” (124 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 Serum problems
Device problems
- Short Fill124
- Incorrect, Inadequate or Imprecise Result or Readings82
- Separation Failure63
- Device Contamination with Chemical or Other Material60
- Leak/Splash55
- Separation Problem46
- Volume Accuracy Problem32
- Device Ingredient or Reagent Problem29
Patient problems
- No Clinical Signs, Symptoms or Conditions436
- No Known Impact Or Consequence To Patient117
- No Consequences Or Impact To Patient32
- No Information7
- No Patient Involvement5
- Hemolysis4
- Exposure to Body Fluids1
- Insufficient Information1
BD Vacutainer Serum models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Vacutainer® Serum 367812Tubes, vials, systems, serum separators, blood collection244 reports
- BD Vacutainer® Serum 367814Tubes, vials, systems, serum separators, blood collection164 reports
- BD Vacutainer® Serum 367820Tubes, vials, systems, serum separators, blood collection148 reports
- BD Vacutainer® Serum 366668Tubes, vials, systems, serum separators, blood collection41 reports
- BD Vacutainer® Serum 366431Tubes, vials, systems, serum separators, blood collection2 reports
Recent BD Vacutainer Serum adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Short Fill
It was reported that when using the BD Vacutainer® Serum Blood Collection Tubes, one (1) tube exhibited backflow, requiring recollection. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946959 ↗MalfunctionSep 29, 2026Short Fill
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50941169 ↗MalfunctionSep 29, 2026Short Fill
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50941160 ↗MalfunctionSep 22, 2026Separation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50862901 ↗MalfunctionSep 10, 2026Short Fill
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50716226 ↗MalfunctionSep 9, 2026Fluid/Blood Leak; Unsealed Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50700880 ↗MalfunctionSep 9, 2026Microbial Contamination of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50695171 ↗MalfunctionMay 28, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, A FOREIGN OBJECT WAS FOUND INSIDE OF ONE TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25319050 ↗MalfunctionMay 27, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, ONE (1) TUBE UNDERFILLED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25309538 ↗MalfunctionMay 18, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES HAD INSUFFICIENT NEGATIVE PRESSURE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25209289 ↗MalfunctionMay 18, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, FOIUR TUBES UNDERFILLED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25202360 ↗MalfunctionMay 18, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, TWO TUBES EXHIBITED INSUFFICIENT NEGATIVE PRESSURE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25201914 ↗MalfunctionMay 7, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, WHITE FLOCCULENT FOREIGN MATTER WAS FOUND IN ONE (1) TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25118878 ↗MalfunctionMay 5, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, ONE (1) TUBE UNDERFILLED DUE TO TUBE PUSH OFF. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25089040 ↗MalfunctionMay 5, 2026Separation Problem
IT WAS REPORTED AFTER USING BD VACUTAINER® SERUM BLOOD COLLECTION TUBES, THE STOPPER POPPED OFF OF ONE (1) TUBE CAUSING THE SAMPLE TO SPILL. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25088904 ↗
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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