BD Vacutainer® Push Button Blood Collection Set 367336Recalls & reported problems
Becton, Dickinson And Company · WINGSET PBBCS 23X.75 7 LUER · Class 2
All models of BD Vacutainer Push Button Blood Collection Set (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This BD Vacutainer push button blood collection set is a winged needle set used to draw blood. Its 152 adverse event reports include 6 injuries and no deaths, and many describe blood leaking from cracked or loose parts and blockages that forced patients to be redrawn. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 152
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 152 adverse event reports that list this exact device (DI 30382903673361), received between Nov 8, 2017 and Sep 30, 2026 — classified as 6 injuries, 146 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (56 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash56
- Fluid/Blood Leak27
- Complete Blockage13
- Difficult or Delayed Activation13
- Product Quality Problem12
- Crack9
- Device Contamination with Chemical or Other Material8
- Device Markings/Labelling Problem5
Patient problems
- No Clinical Signs, Symptoms or Conditions64
- No Known Impact Or Consequence To Patient57
- No Consequences Or Impact To Patient15
- Needle Stick/Puncture5
- No Patient Involvement5
- Discomfort2
- Exposure to Body Fluids2
- Blood Loss1
Recent adverse event reports
The 25 most recent of 152 reports, 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 9, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50692445 ↗MalfunctionApr 20, 2026Detachment of Device or Device Component; Separation Problem
IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, THE COLLECTION SET AND HOLDER SEPARATED.. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24933065 ↗MalfunctionApr 3, 2026Fluid/Blood Leak
IT WAS REPORTED DURING COLLECITON USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, SAMPLE LEAKAGE FROM THE BARREL OF ONE DEVICE WAS OBSERVED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24781049 ↗MalfunctionDec 17, 2025Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE HAD A CRACK IN THE LUER RESULTING IN BLOOD LEAKAGE. THE DEVICE WAS REPLACED. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23835448 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 4 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751822 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 8 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751821 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 9 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751820 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 7 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751819 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 5 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751818 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 10 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751817 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 6 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751814 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 3 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751710 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 2 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751707 ↗MalfunctionDec 8, 2025Complete Blockage; Complete Blockage
PATIENT 1 OF 10: IT WAS REPORTED WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, 1 DEVICE WAS BLOCKED DURING COLLECTION AND PATIENT HAD TO BE REDRAWN. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23751705 ↗MalfunctionNov 10, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BEFORE USING THE BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, SIX (6) UNITS EXHIBITED BLACK FOREIGN MATTER ON THE DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23512478 ↗MalfunctionOct 28, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT BEFORE USING THE BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, FOREIGN MATTER WAS OBSERVED TO BE EMBEDDED IN TEN (10) UNITS. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23403719 ↗MalfunctionAug 28, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHILE USING ONE BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET CUSTOMER NOTICED LEAKAGE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22916516 ↗MalfunctionAug 28, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHILE USING ONE BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, BLOOD LEAKED FROM THE TUBING. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22915358 ↗MalfunctionJun 17, 2025Crack; Leak/Splash; Crack; Leak/Splash
IT WAS REPORTED THAT WHILE USING ONE BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, THE CUSTOMER NOTICED LEAKING FROM THE TUBING. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22237555 ↗MalfunctionJun 12, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHILE USING FOUR BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, BLOOD LEAKED FROM THE SIDE DURING COLLECTION. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22192791 ↗MalfunctionMay 29, 2025Crack; Leak/Splash; Crack; Leak/Splash
IT WAS REPORTED THAT WHILE USING 6 BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, A CRACK IN LUER ADAPTOR WAS SEEN CAUSING LEAKS. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22105240 ↗MalfunctionMay 29, 2025Crack; Leak/Splash; Crack; Leak/Splash
IT WAS REPORTED THAT BEFORE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, THE CUSTOMER NOTICED 250 DEVICES WITH VISIBLE CRACK IN LUER ADAPTOR. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22105225 ↗MalfunctionMay 19, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHILE USING BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET, THE BLOOD FLOWED SLOW, AND THE CUSTOMER NOTICED LEAKAGE AT THE END ON THE NON-PATIENT NEEDLE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22045124 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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