BD™ Universal Viral Transport Flock Mini 220529Recalls & reported problems
Becton, Dickinson And Company · Kit Uvt 3Ml With Flocked Minitip · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 30382902205297), received between Jul 9, 2020 and Jul 2, 2024 — classified as 6 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Break” (8 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
- Break8
- Device Markings/Labelling Problem1
Patient problems
- Foreign Body In Patient8
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 2, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED PRIOR TO USE OF THE BD UNIVERSAL VIRAL TRANSPORT KIT, 3 ML, FLOCKED MINITIP HAD AN UNSPECIFIED NUMBER OF SWABS THAT HAD THE PRINTED DATE ON THE SWAB'S WRAPPER (PEEL POUCH) SHOW THAT IT EXPIRED BEFORE THE EXPIRATION DATE PRINTED ON THE OUTSIDE PACKAGE. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19661233 ↗InjuryOct 8, 2020Break; Break
IT WAS REPORTED WHILE USING BD¿ UNIVERSAL VIRAL TRANSPORT KIT, 3 ML, FLOCKED MINITIP PART OF THE SWAB REMAINED IN THE NASAL CAVITY. SURGICAL INTERVENTION WAS REQUIRED TO REMOVE THE SWAB.
Patient problems: Foreign Body In Patient
MAUDE report 10651400 ↗InjuryAug 18, 2020Break; Break
THE CUSTOMER REPORTED WHILE USING THE KIT UVT 3ML WITH FLOCKED MINITIP FOR SAMPLE COLLECTION THE TIP OF THE SWAB BROKE OFF IN THE PATIENTS NOSE. THE PATIENT RECEIVED AN ENT CONSULT WITH A NASAL ENDOSCOPY AND A CT CHEST SCAN FOR FOREIGN BODIES. IT IS ASSUMED THAT THE TIP WAS SWALLOWED, BUT COULD NOT BE CONFIRMED.
Patient problems: Foreign Body In Patient
MAUDE report 10423567 ↗MalfunctionAug 14, 2020Break; Break
THE CUSTOMER REPORTED WHILE USING THE KIT UVT 3ML WITH FLOCKED MINITIP FOR SAMPLE COLLECTION THE TIP OF THE SWAB BROKE OFF IN THE PATIENTS NOSE. IT IS UNKNOWN HOW THE SWAB WAS REMOVED, BUT THE CUSTOMER INDICATED NO TREATMENT WAS INITIATED. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION WITH NO RESPONSE FROM THE CUSTOMER.
Patient problems: Foreign Body In Patient
MAUDE report 10410469 ↗InjuryAug 14, 2020Break; Break
THE CUSTOMER REPORTED WHILE USING THE KIT UVT 3ML WITH FLOCKED MINITIP FOR SAMPLE COLLECTION THE TIP OF THE SWAB BROKE OFF IN THE PATIENTS NOSE. THE SWAB WAS RETRIEVED USING TWEEZERS BY A PHYSICIAN IN THE EMERGENCY ROOM. THERE WAS NO REPORT OF THE PATIENT REQUIRING ADDITIONAL TREATMENT.
Patient problems: Foreign Body In Patient
MAUDE report 10410468 ↗MalfunctionAug 14, 2020Break; Break
THE CUSTOMER REPORTED WHILE USING THE KIT UVT 3ML WITH FLOCKED MINITIP FOR SAMPLE COLLECTION THE TIP OF THE SWAB BROKE OFF IN THE PATIENTS NOSE. IT IS UNKNOWN HOW THE SWAB WAS REMOVED OR IF IT WAS SWALLOWED. MULTIPLE ATTEMPTS WERE MADE TO OBTAIN ADDITIONAL INFORMATION WITH NO RESPONSE FROM THE CUSTOMER.
Patient problems: Foreign Body In Patient
MAUDE report 10407621 ↗InjuryJul 15, 2020Break; Break
THE CUSTOMER REPORTED WHILE USING THE KIT UVT 3ML WITH FLOCKED MINITIP TO COLLECT A SAMPLE THE TIP OF THE SWAB BROKE OFF IN THE PATIENTS NOSE. THE PATIENT WAS SENT TO THE EMERGENCY ROOM FOR FOLLOW-UP, AND REMOVAL OF THE SWAB. THE PATIENT WAS RELEASED WITH NO FURTHER ISSUES OR TREATMENT NEEDED.
Patient problems: Foreign Body In Patient
MAUDE report 10278600 ↗InjuryJul 10, 2020Break; Break
IT WAS REPORTED WHILE USING A KIT UVT 3ML WITH FLOCKED MINITIP TO COLLECT A SAMPLE THE TIP BROKE OFF IN THE PATIENTS NASAL CAVITY. SEVERAL FOLLOW-UP ATTEMPTS WERE PERFORMED TO OBTAIN ADDITIONAL INFORMATION, BUT THERE WAS NO RESPONSE FROM THE CUSTOMER. IT IS UNKNOWN IF FURTHER MEDICAL INTERVENTION OR TREATMENT WAS REQUIRED.
Patient problems: Foreign Body In Patient
MAUDE report 10257587 ↗InjuryJul 9, 2020Break; Break
IT WAS REPORTED WHILE USING A KIT UVT 3ML WITH FLOCKED MINITIP TO COLLECT A SAMPLE THE TIP BROKE OFF IN THE PATIENTS NASAL CAVITY. SEVERAL FOLLOW-UP ATTEMPTS WERE PERFORMED TO OBTAIN ADDITIONAL INFORMATION, BUT THERE WAS NO RESPONSE FROM THE CUSTOMER. IT IS UNKNOWN IF FURTHER MEDICAL INTERVENTION OR TREATMENT WAS REQUIRED.
Patient problems: Foreign Body In Patient
MAUDE report 10252324 ↗
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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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