BD™ Universal Viral Transport Standard Kit 220221Recalls & reported problems
Becton, Dickinson And Company · Kit Universal Viral Transport Std Swab · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382902202210), received between Aug 14, 2020 and Aug 14, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 14, 2020Break; Break
THE CUSTOMER REPORTED THAT WHILE USING BD¿ UNIVERSAL VIRAL TRANSPORT STD SWAB KIT FOR SAMPLE COLLECTION THE TIP OF THE SWAB BROKE OFF IN THE PATIENT¿S LEFT NOSTRIL. THE SWAB TIP WAS REMOVED DURING A SCHEDULED SURGERY. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION WITH NO RESPONSE FROM THE CUSTOMER.
Patient problems: Foreign Body In Patient
MAUDE report 10410476 ↗
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- BD Vacutainer® Boric Acid Sodium Borate/Formate C&S Urine Tube 364958Becton, Dickinson And Company · CULTURE MEDIA, NON-PROPAGATING TRANSPORT39 reports
- BD Vacutainer® Urine Complete Cup Kit 364956Becton, Dickinson And Company · CULTURE MEDIA, NON-PROPAGATING TRANSPORT38 reports
- BD™ Universal Viral Transport Flock Mini 220529Becton, Dickinson And Company · CULTURE MEDIA, NON-PROPAGATING TRANSPORT9 reports
- BD™ Universal Viral Transport Flock Flex Mini 220531Becton, Dickinson And Company · CULTURE MEDIA, NON-PROPAGATING TRANSPORT6 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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