BD MiniDraw™ SST™ Capillary Blood Collection Tube 366604Recalls & reported problems
Becton, Dickinson And Company · BD MiniDraw™ SST™ Capillary Blood Collection Tube · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This BD MiniDraw SST capillary blood collection tube is a small tube used to collect blood samples from a fingertip. The 38 reports mostly describe sample-quality issues: blood samples reacting improperly in the tube, tubes filling with too little blood, and hemolyzed or clumped samples that had to be redrawn, plus a couple of leaks. None report a death or an injury. There are no recalls for this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 38
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 38 adverse event reports that list this exact device (DI 30382903666042), received between Jul 1, 2024 and Apr 29, 2026 — classified as 38 malfunctions.
The most frequently reported specific device problem is “Improper Chemical Reaction” (19 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
- Improper Chemical Reaction19
- Short Fill8
- Incorrect, Inadequate or Imprecise Result or Readings7
- Leak/Splash2
- Device Ingredient or Reagent Problem1
- Device Markings/Labelling Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions38
Recent adverse event reports
The 25 most recent of 38 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 29, 2026Improper Chemical Reaction
IT WAS REPORTED WHILE USING BD MINIDRAW SST CAPILLARY BLOOD COLLECTION TUBE, PLATELET CLUMPING WAS SEEN WITH ONE PATIENT SAMPLE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25032693 ↗MalfunctionFeb 3, 2026Improper Chemical Reaction
PATIENT 1 OF 2: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, 1 SAMPLE WAS HEMOLYZED. THE SAMPLE WAS RECOLLECTED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24251877 ↗MalfunctionFeb 3, 2026Improper Chemical Reaction
PATIENT 2 OF 2: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, 1 SAMPLE WAS HEMOLYZED. THE SAMPLE WAS RECOLLECTED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24251876 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 4 OF 8 . IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, FIVE TUBES UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240884 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 7 OF 8: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240869 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 6 OF 8: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240868 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 5 OF 8: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240862 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 3 OF 8: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240857 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 8 OF 8 . IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240341 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 2 OF 8: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240332 ↗MalfunctionFeb 2, 2026Short Fill
REPORT 1 OF 8: IT WAS REPORTED WHILE USING BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE TUBE UNDERFILLED RESULTING IN RECOLLECTION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24240331 ↗MalfunctionNov 4, 2025Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS HEMOLYSIS IN THE SAMPLE OF 1 DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23465560 ↗MalfunctionNov 4, 2025Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS HEMOLYSIS IN THE SAMPLE OF 1 DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23465437 ↗MalfunctionSep 12, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS AN INCORRECT PRINTED FILL LINE ON ONE DEVICE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23044312 ↗MalfunctionMay 6, 2025Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS SAMPLE HEMOLYSIS IN ONE DEVICE. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21969408 ↗MalfunctionMay 6, 2025Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS SAMPLE HEMOLYSIS IN ONE DEVICE. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21969393 ↗MalfunctionFeb 25, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT AFTER SAMPLE COLLECTION WITH THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, THE SAMPLE HEMOLYZED IN ONE (1) UNIT. NO RECOLLECTION WAS COMPLETED ON THE PATIENT. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21459255 ↗MalfunctionFeb 12, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED WHILE USING BD MINIDRAW¿ FINGER SLEEVE, EXTRA-LARGE, THERE WAS SAMPLE LEAKAGE FROM ONE (1) TUBE. THE PATIENT PASSING OUT AT THE SIGHT OF BLOOD. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21370123 ↗MalfunctionJan 3, 2025Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS 1 SAMPLE EXHIBITING HEMOLYSIS. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21066588 ↗MalfunctionDec 13, 2024Device Ingredient or Reagent Problem; Device Ingredient or Reagent Problem
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS POOR GEL BARRIER FORMATION ON 1 DEVICE. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20925624 ↗MalfunctionDec 13, 2024Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS HEMOLYSIS OF ONE SAMPLE. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20924615 ↗MalfunctionDec 6, 2024Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS HEMOLYSIS OF ONE SAMPLE. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20869095 ↗MalfunctionDec 2, 2024Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS HEMOLYSIS OF ONE SAMPLE. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20825097 ↗MalfunctionDec 2, 2024Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE THERE WAS HEMOLYSIS OF ONE SAMPLE. THE SAMPLE WAS RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20825089 ↗MalfunctionNov 22, 2024Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ SST¿ CAPILLARY BLOOD COLLECTION TUBE, ONE BLOOD SAMPLE WAS HEMOLYZED AND NEEDED TO BE RECOLLECTED. THERE WERE NO OTHER HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20762212 ↗
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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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