BD SurePrep™ Capillary Tubes- PLAIN 420315Recalls & reported problems
Becton, Dickinson And Company · BD SurePrep™ Capillary Tubes- PLAIN · Class 1
Data updated Oct 13, 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 30382904203154), received between May 20, 2022 and May 20, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Fluid/Blood Leak1
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.
MalfunctionMay 20, 2022Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT WHILE USING BD SUREPREP¿ CAPILLARY TUBES- PLAIN THE CUSTOMER OBSERVED LEAKAGE FROM TUBES AFTER CENTRIFUGATION. THIS EVENT OCCURRED 1 TIME(S). THERE IS NO INDICATION THAT FALSE RESULTS WERE REPORTED TO HEALTH CARE PRACTITIONERS. THERE IS NO INDICATION OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CUSTOMER REPORTS 20-50% LEAKAGE ON CENTRIFUGATION FROM THE ¿SEALED¿ END OF THE CAPILLARY TUBE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14458891 ↗
Other TUBE, COLLECTION, CAPILLARY BLOOD devices
- Globe Scientific 51635Globe Scientific Inc. · Tube, Collection, Capillary Blood1 recall1 report
- CardioChek 5700534Henry Schein, Inc. · TUBE, COLLECTION, CAPILLARY BLOOD1 recall0 reports
- SAFE-T-FILL® 06 0005Ram Scientific, Inc · TUBE, COLLECTION, CAPILLARY BLOOD1 recall0 reports
- SAFE-T-FILL® 06 0185Ram Scientific, Inc · TUBE, COLLECTION, CAPILLARY BLOOD1 recall0 reports
- SAFE-T-FILL® 06 0009Ram Scientific, Inc · TUBE, COLLECTION, CAPILLARY BLOOD1 recall0 reports
- SAFE-T-FILL® 06 0007Ram Scientific, Inc · TUBE, COLLECTION, CAPILLARY BLOOD1 recall0 reports
- SAFE-T-FILL® 06 0186Ram Scientific, Inc · TUBE, COLLECTION, CAPILLARY BLOOD1 recall0 reports
- SAFE-T-FILL® 06 0187Ram Scientific, Inc · TUBE, COLLECTION, CAPILLARY BLOOD1 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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