BD Vacutainer K2 EDTA (K2E) 10.8mg Blood Collection TubesRecalls & reported problems across all models
Becton, Dickinson And Company · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 360
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls
- 0
We found 2 models of BD Vacutainer K2 EDTA (K2E) 10.8mg Blood Collection Tubes by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 360 adverse event reports in the FDA's MAUDE database, received between Dec 4, 2017 and Jun 11, 2026 — classified as 3 injuries, 357 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (117 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 K2 EDTA (K2E) 10.8mg Blood Collection Tubes problems
Device problems
- Device Contamination with Chemical or Other Material117
- Leak/Splash45
- Short Fill44
- Incorrect Or Inadequate Test Results30
- Incorrect, Inadequate or Imprecise Result or Readings29
- Device Markings/Labelling Problem22
- Device Ingredient or Reagent Problem17
- Volume Accuracy Problem16
Patient problems
- No Known Impact Or Consequence To Patient143
- No Clinical Signs, Symptoms or Conditions129
- No Patient Involvement48
- No Consequences Or Impact To Patient29
- No Information11
- Exposure to Body Fluids1
- Hemolysis1
BD Vacutainer K2 EDTA (K2E) 10.8mg Blood Collection Tubes models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Vacutainer® K2 EDTA (K2E) 10.8mg Blood Collection Tubes 367863Tubes, vials, systems, serum separators, blood collection268 reports
- BD Vacutainer® K2 EDTA (K2E) 10.8mg Blood Collection Tubes 367899Tubes, vials, systems, serum separators, blood collection92 reports
Recent BD Vacutainer K2 EDTA (K2E) 10.8mg Blood Collection Tubes adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 11, 2026Coagulation in Device or Device Ingredient
IT WAS REPORTED THAT DURING THE USE OF BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBE, ONE (1) TUBE APPEARED TO BE CLOTTED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENTS OR USERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25476957 ↗MalfunctionJun 10, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BEFORE THE USE OF THE BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, ONE (1) TUBE WAS FOUND TO CONTAIN GREEN PARTICLE INSIDE THE TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25453102 ↗MalfunctionMay 26, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, SIX TUBES HAVE SMALL HOLES IN THEM RESULTING IN SAMPLE LEAKAGE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25285251 ↗MalfunctionMay 12, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES CONTAINED FOREIGN MATTER. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25153515 ↗MalfunctionApr 30, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES UNDERFILLED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25052782 ↗MalfunctionMar 3, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, 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 24503557 ↗MalfunctionFeb 9, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, FOREIGN MATTER WAS FOUND EMBEDDED IN 51 TUBES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24299194 ↗MalfunctionJan 28, 2026Improper or Incorrect Procedure or Method
IT WAS REPORTED WHILE USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES WERE USED AFTER THE EXPIRATION DATE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24203743 ↗MalfunctionDec 4, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, FOREIGN MATTER WAS FOUND IN TWO (2) TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23723065 ↗MalfunctionOct 30, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, FOREIGN MATTER- HAIR 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 23425903 ↗MalfunctionOct 28, 2025Excessive Heating; Excessive Heating
IT WAS REPORTED THAT PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED TEMPERATURE EXCURSION DURING TRANSPORT. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23410093 ↗MalfunctionOct 28, 2025Excessive Heating; Excessive Heating
IT WAS REPORTED THAT PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED TEMPERATURE EXCURSION DURING TRANSPORT. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23410091 ↗MalfunctionSep 16, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, 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 23069456 ↗MalfunctionSep 15, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, FOREIGN MATTER WAS FOUND IN TWO (2) TUBES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23052936 ↗MalfunctionSep 5, 2025Excessive Heating; Excessive Heating
IT WAS REPORTED PRIOR TO USE OF BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES, AN UNSPECIFIED NUMBER OF TUBES WERE STORED AT INCORRECT TEMPERATURE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22977606 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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