BD MiniDraw™ Finger Sleeve, Small 366613Recalls & reported problems
Becton, Dickinson And Company · BD MiniDraw™ Finger Sleeve, Small · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 30382903666134), received between Jun 28, 2024 and Oct 29, 2025 — classified as 12 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (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
- Leak/Splash8
- Device Contamination with Body Fluid3
- Expiration Date Error1
Patient problems
- No Clinical Signs, Symptoms or Conditions12
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 2 OF 3: IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THERE WAS 1 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 23411414 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 3 OF 3: IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THERE WAS 1 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 23410689 ↗MalfunctionOct 29, 2025Leak/Splash; Leak/Splash
REPORT 2 OF 2: IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, 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 23410663 ↗MalfunctionMar 28, 2025Device Contamination with Body Fluid; Device Contamination with Body Fluid
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE SMALL, THERE WAS RESIDUAL BLOOD WITHIN TWO DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21718706 ↗MalfunctionMar 19, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THERE WERE THREE (3) 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 21642822 ↗MalfunctionMar 18, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THERE WERE THREE (3) 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 21632617 ↗MalfunctionFeb 25, 2025Leak/Splash; Leak/Splash
IT WAS REPORTED THAT WHEN USING ONE (1) BD MINIDRAW FINGER SLEEVE, SMALL, BLOOD WAS LEAKING OUT OF THE SLEEVE CAUSING AN UNDERFILLED SAMPLE. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21458762 ↗MalfunctionJan 2, 2025Device Contamination with Body Fluid; Device Contamination with Body Fluid
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL SAMPLE WAS LEAKING OUT THE FRONT AND BACK OF 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 21060119 ↗MalfunctionNov 27, 2024Leak/Splash; Leak/Splash
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THERE WAS SAMPLE (BLOOD) POOLING WITHIN AN UNSPECIFIED NUMBER OF DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20795876 ↗MalfunctionNov 27, 2024Leak/Splash; Leak/Splash
IT WAS REPORTED WHILE USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THERE WAS SAMPLE (BLOOD) POOLING WITHIN 4 DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20793425 ↗MalfunctionAug 6, 2024Expiration Date Error; Expiration Date Error
IT WAS REPORTED BEFORE USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL, THE EXPIRATION DATE ON THE PACKAGING LABEL WAS BEYOND THE SPECIFIED PRODUCT SHELF LIFE. THE EVENT AFFECTED 3600 DEVICES. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19924144 ↗MalfunctionJun 28, 2024Device Contamination with Body Fluid; Device Contamination with Body Fluid
IT WAS REPORTED WHEN USING THE BD MINIDRAW¿ FINGER SLEEVE, SMALL THERE WAS BLOOD POOLING. THERE WERE NO HEALTH CONSEQUENCES OR IMPACTS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19637129 ↗
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- Cyto-Chex BCT 213559Streck, Inc. · Tubes, Vacuum Sample, With Anticoagulant1 recall0 reports
- Vacuette 454332Greiner Bio-One GmbH · Tubes, vacuum sample, with anticoagulant1 recall0 reports
- Cyto-Chex BCT 218980Streck, Inc. · Tubes, Vacuum Sample, With Anticoagulant1 recall0 reports
- Vacuette 454334Greiner Bio-One GmbH · Tubes, vacuum sample, with anticoagulant1 recall0 reports
- BD MiniDraw™ Finger Sleeve, Extra-Large 366616Becton, Dickinson And Company · Tubes, vacuum sample, with anticoagulant25 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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