BD Vacutainer® Z (No Additive) Plus Urine Tube 368501Recalls & reported problems
Becton, Dickinson U.K. Limited · TUBE URIN PLH 13X100 6.0 UA TAN · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30382903685012), received between Jul 16, 2024 and Jun 18, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (2 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
- Device Contamination with Chemical or Other Material2
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 18, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED BEFORE USING THE BD VACUTAINER® Z (NO ADDITIVE) PLUS URINE TUBE THERE WAS FOREIGN MATTER INSIDE 15 DEVICES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22284693 ↗MalfunctionMar 5, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED AFTER USING BD VACUTAINER® Z (NO ADDITIVE) PLUS URINE TUBE FOREIGN MATTER WAS FOUND INSIDE THE TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21528954 ↗MalfunctionJul 16, 2024Leak/Splash; Leak/Splash
IT WAS REPORTED WHEN USING THE BD VACUTAINER® Z (NO ADDITIVE) PLUS URINE TUBE, THE TUBE BROKE IN THE CENTRIFUGE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19754809 ↗
Other CONTAINER, SPECIMEN, STERILE devices
- BD Vacutainer® Urine Analysis Preservative Tube 364992Becton, Dickinson And Company · CONTAINER, SPECIMEN, STERILE160 reports
- Medline Industries, Inc. DYNJ50241CMedline Industries, Inc. · CONTAINER, SPECIMEN, STERILE3 recalls0 reports
- BD Vacutainer® No Additive (Z) Tubes 366703Becton, Dickinson And Company · CONTAINER, SPECIMEN, STERILE143 reports
- Medline Industries, Inc. DYNJ63118AMedline Industries, Inc. · CONTAINER, SPECIMEN, STERILE2 recalls0 reports
- MyCareLink Smart™ 25000Medtronic, Inc. · CONTAINER, SPECIMEN, STERILE1 recall5 reports
- Centurion MG912STCenturion Medical Products Corporation · CONTAINER, SPECIMEN, STERILE1 recall0 reports
- Vacuette 450225Greiner Bio-One GmbH · CONTAINER, SPECIMEN, STERILE1 recall0 reports
- Medline Industries, Inc. DYNJ905664IMedline Industries, Inc. · CONTAINER, SPECIMEN, STERILE1 recall0 reports
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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