BD Vacutainer® UltraTouch™ Push Button Blood Collection Set with PAH 368685Recalls & reported problems
Becton, Dickinson And Company · UT-PBBCS 23G 7 PAH CE · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This BD Vacutainer UltraTouch push button blood collection set is used to draw blood samples. Most of the 82 reports describe blood leaking from the tubing, sleeve, or adapter. The reports include no injuries and no deaths, and reports rose from 3 in the previous 12 months to 79 in the last 12 months. 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
- 77
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 77 adverse event reports that list this exact device (DI 30382903686859), received between Nov 8, 2024 and Aug 17, 2026 — classified as 77 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (61 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak61
- Leak/Splash15
- Material Split, Cut or Torn5
- Volume Accuracy Problem2
- Packaging Problem1
- Retraction Problem1
- Short Fill1
Patient problems
- No Clinical Signs, Symptoms or Conditions71
- Exposure to Body Fluids4
- Discomfort2
- Pain2
Recent adverse event reports
The 25 most recent of 77 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 17, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50278297 ↗MalfunctionApr 29, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD IS LEAKING FROM THE LUER ADAPTER OF AN UNSPECIFIED NUMBER OF DEVICES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25034818 ↗MalfunctionApr 29, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THE TUBING OF AN UNSPECIFIED NUMBER OF DEVICES LEAKED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25034805 ↗MalfunctionApr 27, 2026Short Fill
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, TUBING WAS PINCHED RESULTING IN POOR BLOOD FLOW. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25009426 ↗MalfunctionApr 23, 2026Retraction Problem
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THE NON PATIENT NEEDLE SLEEVE WAS PIERCED BY THE NEEDLE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24972267 ↗MalfunctionApr 23, 2026Fluid/Blood Leak; Material Split, Cut or Torn
REPORT 4 OF 4: IT WAS REPORTED THAT DURING COLLECTION OF ONE PATIENT USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, A HOLE IN THE TUBING RESULTED IN SAMPLE LEAKAGE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24968291 ↗MalfunctionApr 23, 2026Fluid/Blood Leak; Material Split, Cut or Torn
REPORT 2 OF 4: IT WAS REPORTED THAT DURING COLLECTION OF ONE PATIENT USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, A HOLE IN THE TUBING RESULTED IN SAMPLE LEAKAGE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24968267 ↗MalfunctionApr 23, 2026Fluid/Blood Leak; Material Split, Cut or Torn
REPORT 1 OF 4: IT WAS REPORTED THAT DURING COLLECTION OF ONE PATIENT USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, A HOLE IN THE TUBING RESULTED IN SAMPLE LEAKAGE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24968239 ↗MalfunctionApr 23, 2026Fluid/Blood Leak; Material Split, Cut or Torn
REPORT 3 OF 4: IT WAS REPORTED THAT DURING COLLECTION OF ONE PATIENT USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, A HOLE IN THE TUBING RESULTED IN SAMPLE LEAKAGE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24968229 ↗MalfunctionApr 20, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING [BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE TUBING OF THE DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24934037 ↗MalfunctionApr 20, 2026Fluid/Blood Leak
REPORT 1 OF 2 IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE TUBING OF THE DEVICE WITH ONE (1) PATIENT. THE PATIENT HAD TO HAVE AN ADDITIONAL NEEDLESTICK FOR THE DRAW. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: Discomfort; Pain
MAUDE report 24933480 ↗MalfunctionApr 20, 2026Fluid/Blood Leak
REPORT 2 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE TUBING OF THE DEVICE WITH ONE (1) PATIENT. THE PATIENT HAD TO HAVE AN ADDITIONAL NEEDLESTICK FOR THE DRAW. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: Discomfort; Pain
MAUDE report 24933477 ↗MalfunctionApr 17, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, SAMPLE LEAKAGE OCCURS WITH AN UNSPECIFIED NUMBER OF DEVICES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24915760 ↗MalfunctionApr 17, 2026Fluid/Blood Leak
IT WAS REPORTED THAT WHILE USING THE VACUTAINER ULTRATOUCH THAT THE DEVICE SET LEAKED INTO THE HOSE DOWN TO THE VACUTAINER. THIS OCCURRED IN AN UNSPECIFIED AMOUNT OF DEVICES. NO PATIENT IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24911006 ↗MalfunctionApr 16, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THERE WAS A HOLE IN THE TUBING OF ONE DEVICE RESULTING IN SAMPLE LEAKAGE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24903881 ↗MalfunctionApr 16, 2026Fluid/Blood Leak
IT WAS REPORTED THAT WHEN USING THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, ONE (1) UNIT EXHIBITED BLOOD LEAKAGE AT LUER. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24900019 ↗MalfunctionApr 8, 2026Fluid/Blood Leak
REPORT 2 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THERE IS A HOLE IN THE TUBING OF AN UNSPECIFIED NUMBER OF DEVICES RESULTING IN SAMPLE LEAKAGE AND THE PATIENTS HAVING TO BE RE-PRICKED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24821967 ↗MalfunctionApr 8, 2026Fluid/Blood Leak
REPORT 1 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THERE IS A HOLE IN THE TUBING OF ONE DEVICE RESULTING IN SAMPLE LEAKAGE AND THE PATIENT HAVING TO BE RE-PRICKED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24821803 ↗MalfunctionApr 7, 2026Fluid/Blood Leak
REPORT 2 OF 2. IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE TUBING OF THE DEVICE. THIS OCCURRED AN UNSPECIFIED NUMBER OF TIMES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24809043 ↗MalfunctionApr 7, 2026Fluid/Blood Leak
REPORT 1 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE TUBING OF THE DEVICE. THIS OCCURRED AN UNSPECIFIED NUMBER OF TIMES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24809042 ↗MalfunctionApr 3, 2026Fluid/Blood Leak
IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE NON-PATIENT END OF THE DEVICE AT THE CONNECTION BETWEEN THE HUB AND SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24780425 ↗MalfunctionApr 3, 2026Fluid/Blood Leak; Volume Accuracy Problem
REPORT 2 OF 3: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE HUB OF THE DEVICE WHEN ATTEMPTING TO DRAW INTO A BLOOD COLLECTION TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24780222 ↗MalfunctionApr 2, 2026Fluid/Blood Leak
REPORT 1 OF 3: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE HUB OF THE DEVICE WHEN ATTEMPTING TO DRAW INTO A BLOOD COLLECTION TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24771270 ↗MalfunctionApr 2, 2026Fluid/Blood Leak; Volume Accuracy Problem
REPORT 3 OF 3. IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD LEAKED FROM THE HUB OF THE DEVICE WHEN ATTEMPTING TO DRAW INTO A BLOOD COLLECTION TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24771252 ↗MalfunctionApr 2, 2026Fluid/Blood Leak
REPORT 2 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, BLOOD FROM AN UNSPECIFIED NUMBER OF DEVICES LEAKED BETWEEN THE TUBE AND THE HOLDER. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24770152 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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