Skip to content

BD MiniDraw™ H&H Capillary Blood Collection Tube 366603Recalls & reported problems

Becton, Dickinson And Company · BD MiniDraw™ H&H Capillary Blood Collection Tube · Class 2

Quick summary

This BD MiniDraw capillary blood collection tube is a small tube used to collect blood samples with an anticoagulant. Its 141 reports mostly describe samples that clotted or showed platelet clumping. There are no deaths and no injuries. No recalls name 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
141
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 141 adverse event reports that list this exact device (DI 50382903666039), received between Jun 8, 2024 and Jul 27, 2026 — classified as 141 malfunctions.

The most frequently reported specific device problem is “Coagulation in Device or Device Ingredient” (91 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 16 reportsJul 2024: 9 reportsAug 2024: 16 reportsSep 2024: 13 reportsOct 2024: 1 reportsNov 2024: 5 reportsDec 2024: 6 reportsJan 2025: 3 reportsFeb 2025: 0 reportsMar 2025: 8 reportsApr 2025: 0 reportsMay 2025: 4 reportsJun 2025: 0 reportsJul 2025: 15 reportsAug 2025: 0 reportsSep 2025: 3 reportsOct 2025: 1 reportsNov 2025: 5 reportsDec 2025: 6 reportsJan 2026: 0 reportsFeb 2026: 13 reportsMar 2026: 0 reportsApr 2026: 16 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 1 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports20242025202616
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Coagulation in Device or Device Ingredient91
  • Clumping in Device or Device Ingredient54
  • Improper Chemical Reaction30
  • Incorrect, Inadequate or Imprecise Result or Readings1
  • Leak/Splash1

Patient problems

  • No Clinical Signs, Symptoms or Conditions141

Recent adverse event reports

The 25 most recent of 141 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 27, 2026Improper Chemical Reaction

    Patient 28 of 30:It was reported while using BD MiniDraw¿ H&H Capillary Blood Collection Tube, 1 sample exhibited platelet clumping. There was no health impact or consequences reported.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50045810 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032715 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032711 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032181 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032177 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H CAPILLARY BLOOD COLLECTION TUBE, CLOTTING 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 25032174 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032172 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032169 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032164 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032155 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032151 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032146 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032112 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032106 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032099 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25032060 ↗
  • MalfunctionApr 29, 2026Improper Chemical Reaction

    IT WAS REPORTED WHILE USING BD MINIDRAW H&H 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 25031978 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient

    PATIENT 2 OF 2: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 SAMPLE WAS CLOTTED. THE SAMPLE WAS RECOLLECTED IF THE PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254252 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 9 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254251 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 1 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254250 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 8 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254249 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 7 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254248 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 2 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254247 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 4 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254238 ↗
  • MalfunctionFeb 3, 2026Coagulation in Device or Device Ingredient; Improper Chemical Reaction

    PATIENT 5 OF 9: IT WAS REPORTED WHILE USING BD MINIDRAW¿ H&H CAPILLARY BLOOD COLLECTION TUBE, 1 PATIENT SAMPLE HAD PLATELET AGGREGATES. A RECOLLECT WAS PERFORMED IF PATIENT AGREED. THERE WAS NO OTHER HEALTH IMPACT OR CONSEQUENCES REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24254237 ↗

Other Tubes, vacuum sample, with anticoagulant devices

All Tubes, vacuum sample, with anticoagulant devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.