BD Vacutainer® Urinalysis Transfer Straw Kit 364943Recalls & reported problems
Becton, Dickinson And Company · KIT URIN TRANSTR 16X100 8.0 UAP RD/YEL · Class 1
All models of BD Vacutainer Urinalysis Transfer Straw Kit (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 30382903649434), received between Apr 12, 2022 and Aug 13, 2025 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Product Quality Problem” (3 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
- Product Quality Problem3
- Break1
- Component Missing1
- Loss of or Failure to Bond1
- Material Discolored1
- Separation Problem1
- Short Fill1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 13, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED BEFORE USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT THE CANNULA SEPARATED FROM THE STRAW ON TWO DEVICES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22797166 ↗MalfunctionMar 12, 2025Separation Problem; Separation Problem
IT WAS REPORTED THAT PRIOR TO USING BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT, THE STRAW OF AN UNSPECIFIED NUMBER OF DEVICES EITHER BREAKS OFF, BENDS, OR PULLS OUT WITH THE NEEDLE STILL ATTACHED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21584367 ↗MalfunctionOct 11, 2024Break; Break
IT WAS REPORTED BEFORE USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT ONE STRAW SEPARATED FROM THE HOLDER. ADDITIONALLY ONE KIT HAD A HALF A STRAW MISSING WHILE ANOTHER KIT HAD HALF A STRAW EXTRA. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20434306 ↗MalfunctionNov 9, 2023Component Missing; Component Missing
IT WAS REPORTED WHEN USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT CUSTOMER THEY ONLY RECEIVED THE STRAW BUT NOT THE CONICAL TUBE. NO PATIENT IMPACTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: CUSTOMER PROBLEM: CUSTOMER IS REPORTING THEY ONLY RECEIVED THE STRAW BUT NOT THE CONICAL TUBE. AFFECTED LOT NUMBER 3062535.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18100273 ↗MalfunctionJun 27, 2023Product Quality Problem; Product Quality Problem
IT WAS REPORTED WHEN USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT THE CUSTOMER NEEDLE IS EXPOSED THROUGH PACKAGING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "IT WAS REPORTED BY THE CUSTOMER THAT NEEDLE EXPOSED THROUGH PACKAGING. CUSTOMER STATES EXPOSED NEEDLE SEEN THROUGH PACKAGING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17210455 ↗MalfunctionAug 19, 2022Short Fill; Short Fill
IT WAS REPORTED WHEN USING THE UNSPECIFIED BD VACUTAINER TUBE THERE WAS UNDER-FILL OR LOW DRAW OF A TUBE WITH BLOOD. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "THE RED TOP SERUM TUBES ARE FILLING SLOWLY."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15259984 ↗MalfunctionAug 12, 2022Product Quality Problem; Product Quality Problem
IT WAS REPORTED WHEN USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT THERE WAS A MISSING COMPONENT.THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "THE URINE NEEDLE IS MISSING SAFETY SHIELD."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15221463 ↗MalfunctionAug 1, 2022Product Quality Problem; Product Quality Problem
IT WAS REPORTED WHEN USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT THERE WAS MISSING COMPONENT OF THE PRODUCT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "ONE TRANSFER STRAW WAS MISSING THE HOLDER/SAFETY DEVICE OVER THE NEEDLE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15141361 ↗MalfunctionApr 12, 2022Material Discolored; Material Discolored
IT WAS REPORTED WHEN USING THE BD VACUTAINER® URINALYSIS TRANSFER STRAW KIT THERE WAS DISCOLORED/ABNORMAL ADDITIVE FORM. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: WE "OBSERVED COLOR CHANGES IN THE TUBES."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14090145 ↗
Other SYSTEM, TRANSPORT, AEROBIC devices
- BD Vacutainer® Urine Complete Cup Kit 364957Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC1 recall5 reports
- BBL™ CultureSwab™ EZ 220144Copan Italia SPA · System, Transport, Aerobic1 recall0 reports
- BD Vacutainer® Urine Transfer Straw 364966Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC22 reports
- BD Vacutainer® Urinalysis Transfer Straw Kit 364990Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC11 reports
- BD Vacutainer® Urinalysis Cup Kit 364946Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC11 reports
- BD Vacutainer® Urine Collection Cups 364975Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC10 reports
- BD Vacutainer® Urinalysis Cup Kit 364981Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC5 reports
- BD Vacutainer® Urinalysis Cup Kit 364989Becton, Dickinson And Company · SYSTEM, TRANSPORT, AEROBIC3 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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