BD Vacutainer® Urinalysis Conical Urine Tube 364980Recalls & reported problems
Becton, Dickinson And Company · TUBE URIN PLC 16X100 8.0 CONI UA YEL · 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 30382903649809), received between Dec 11, 2025 and May 26, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (1 report).
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 Material1
- Device Markings/Labelling Problem1
- Material Deformation1
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.
MalfunctionMay 26, 2026Device Contamination with Chemical or Other Material
IT WAS REPORTED WHILE USING BD VACUTAINER® URINALYSIS CONICAL URINE TUBE NO ADDITIVE, FOREIGN MATTER WAS OBSERVED IN ONE TUBE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25292075 ↗MalfunctionMay 11, 2026Device Markings/Labelling Problem
IT WAS REPORTED PRIOR TO USING BD VACUTAINER® URINALYSIS CONICAL URINE TUBE, AN UNSPECIFIED NUMBER OF TUBES HAD AN INCORRECT LABEL. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25144077 ↗MalfunctionDec 11, 2025Material Deformation; Material Deformation
IT WAS REPORTED WHILE USING BD VACUTAINER® SST¿, THE EDGES OF TWO (2) TUBE CAPS ARE UNEVEN. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23780070 ↗
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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