BD MiniDraw™ Finger Sleeve, Medium 366614Recalls & reported problems
Becton, Dickinson And Company · BD MiniDraw™ Finger Sleeve, Medium · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 19
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 19 adverse event reports that list this exact device (DI 30382903666141), received between Jun 28, 2024 and Oct 29, 2025 — classified as 19 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (16 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
- Leak/Splash16
- Device Contamination with Body Fluid2
- Expiration Date Error1
Patient problems
- No Clinical Signs, Symptoms or Conditions19
Recent adverse event reports
The 19 most recent of 19 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 3 OF 3: IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS RESIDUAL BLOOD IN ONE DEVICE. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23411712 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 2 OF 3: IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS RESIDUAL BLOOD IN ONE DEVICE. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23410833 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 3 OF 4: IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE WAS ONE INSTANCE OF BLOOD POOLING IN THE FINGER SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23410688 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 3 OF 4:IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE WAS ONE INSTANCE OF BLOOD POOLING IN THE FINGER SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23410678 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 2 OF 4: IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE WAS ONE INSTANCE OF BLOOD POOLING IN THE FINGER SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23410656 ↗MalfunctionApr 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS RESIDUAL BLOOD IN ONE DEVICE. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21774833 ↗MalfunctionApr 4, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS RESIDUAL BLOOD IN ONE DEVICE. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21774464 ↗MalfunctionMar 28, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS RESIDUAL BLOOD IN THREE DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21724331 ↗MalfunctionMar 21, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING ONE (1) BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, BLOOD WAS POOLING IN THE FINGER SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21667848 ↗MalfunctionMar 19, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE WERE FOUR (4) INSTANCES OF BLOOD POOLING IN THE FINGER SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21641416 ↗MalfunctionMar 11, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING ONE (1) BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, BLOOD WAS POOLING IN THE FINGER SLEEVE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21580322 ↗MalfunctionMar 7, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING ONE (1) BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE IS BLOOD SMEARING. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21548028 ↗MalfunctionMar 7, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING ONE (1) BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE IS BLOOD SMEARING BY POOLING IN THE FINGER SLEEVE AND NEVER DRIPPING INTO THE TUB. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21547859 ↗MalfunctionFeb 26, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, BLOOD WAS SMEARING IN THE SLEEVE, TOWARD THE PALM, CAUSING THE SLEEVE TO COME OFF OF THE FINGER AFTER EVERY SQUEEZE ON FOUR (4) UNITS. THE SAMPLE WAS RECOLLECTED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21468844 ↗MalfunctionDec 4, 2024Leak/Splash; Leak/Splash
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS SAMPLE LEAKING FROM AN UNSPECIFIED NUMBER OF DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20844187 ↗MalfunctionNov 27, 2024Leak/Splash; Leak/Splash
IT WAS REPORTED WHILE USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THERE WAS SAMPLE (BLOOD) POOLING WITHIN 7 DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20793391 ↗MalfunctionAug 6, 2024Expiration Date Error; Expiration Date Error
IT WAS REPORTED BEFORE USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM, THE EXPIRATION DATE ON THE PACKAGING LABEL WAS BEYOND THE SPECIFIED PRODUCT SHELF LIFE. THE EVENT AFFECTED 4860 DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19923047 ↗MalfunctionJun 28, 2024Device Contamination with Body Fluid; Device Contamination with Body Fluid
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS BLOOD POOLING. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19638429 ↗MalfunctionJun 28, 2024Device Contamination with Body Fluid; Device Contamination with Body Fluid
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, MEDIUM THERE WAS BLOOD POOLING. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19636754 ↗
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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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