Midstream Urine Collector 842803Recalls & reported problems
C. R. Bard, Inc. · Midstream Urine Collector with Rigid Funnel and Castille Soap Towelettes · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741051210), received between Jun 25, 2021 and Jun 25, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Tear, Rip or Hole in Device Packaging” (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.
Most reported problems
Device problems
- Tear, Rip or Hole in Device Packaging1
- Unsealed Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 25, 2021Unsealed Device Packaging; Tear, Rip or Hole in Device Packaging; Unsealed Device Packaging; Tear, Rip or Hole in Device Packaging
IT WAS REPORTED THAT GLUE THAT KEEPS THE MIDSTREAM BOXES CLOSED WAS NOT GLUED SHUT AND THE MIDSTREAM FELL TO THE GROUND.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12071112 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page