BD Vacutainer® UltraTouch™ Push Button Blood Collection Set with PAH 368687Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 30382903686873), received between Aug 23, 2024 and Mar 23, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Unsealed Device Packaging” (4 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.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 23, 2026Unsealed Device Packaging

  IT WAS REPORTED WHILE USING BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THE INDIVIDUAL PACKAGING OF 100 DEVICES WAS ALREADY OPENED WHEN THE BOX WAS UNPACKED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24662639 ↗
• MalfunctionJan 13, 2026Unsealed Device Packaging

  IT WAS REPORTED THAT UPON RECEIPT OF THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THE CUSTOMER OBSERVED THAT 80 UNITS OF THE COLLECTION SET PACKAGES WERE NOT SEALED. NO PATIENT OR USER IMPACT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24063715 ↗
• MalfunctionJan 13, 2026Unsealed Device Packaging

  IT WAS REPORTED THAT UPON RECEIPT OF THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH, THE CUSTOMER OBSERVED THAT 100 UNITS OF THE COLLECTION SET PACKAGES WERE NOT SEALED. NO PATIENT OR USER IMPACT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24053715 ↗
• MalfunctionDec 19, 2025Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT WHILE USING THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH THAT THE INDIVIDUAL PACKAGING WAS ALREADY OPENED WHEN THE BOX WAS UNPACKED. THIS OCCURRED IN 20 DEVICES. NO PATIENT IMPACT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23857153 ↗
• MalfunctionNov 7, 2025Short Fill; Short Fill

  IT WAS REPORTED WHEN USING THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH THERE WAS AIR DRAWING INTO 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 23501679 ↗
• MalfunctionNov 3, 2025Packaging Problem; Packaging Problem

  IT WAS REPORTED BEFORE USING THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH 120 DEVICES WERE DELIVERED WITH BLISTER PACKS UNSEALED RENDERING THEM NON-STERILE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23458847 ↗
• MalfunctionOct 30, 2025Unsealed Device Packaging; Unsealed Device Packaging

  IT WAS REPORTED BEFORE USING THE BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH THERE AN UNSEALED BLISTER PACK ON 30 DEVICES RENDERING THEM NON-STERILE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23425189 ↗
• MalfunctionAug 23, 2024Packaging Problem; Packaging Problem

  IT WAS REPORTED PRIOR TO USE OF BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET WITH PAH THE PACKAGING FOR 10 DEVICES ARE OPEN AND STERILITY IS COMPROMISED. IT ALSO APPEARS THE PRODUCT WAS INVERTED IN THE PACKAGING. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20045217 ↗