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BD Vacutainer® Stretch Latex Free Tourniquet 367203Recalls & reported problems

Becton, Dickinson And Company · TOURNIQUET STRETCH LATEX FREE · Class 1

Adverse event reports
3
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30382903672036), received between Dec 5, 2017 and Jan 14, 2022 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (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

  • Device Markings/Labelling Problem1
  • Missing Information1
  • Patient-Device Incompatibility1

Patient problems

  • Headache1
  • Hypersensitivity/Allergic reaction1
  • No Clinical Signs, Symptoms or Conditions1
  • No Known Impact Or Consequence To Patient1
  • Reaction1
  • Skin Irritation1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 14, 2022Missing Information; Missing Information

    IT WAS REPORTED WHEN USING THE BD TOURNIQUET STRETCH LATEX FREE, THE DEVICE EXPERIENCED NO LABEL OR MISSING LABEL INFORMATION. THIS EVENT OCCURRED 5 TIMES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: 5 UNITS OF THE PRODUCT HAVE BEEN DELIVERED TO CUSTOMER WITHOUT BATCH # AND NO EXP. DATE EITHER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13260529 ↗
  • MalfunctionJun 18, 2018Device Markings/Labelling Problem; Device Markings/Labelling Problem

    IT WAS REPORTED THAT BD VACUTAINER® STRETCH LATEX FREE TOURNIQUET HAD MISSING AND UNREADABLE LABEL INFORMATION. NO SERIOUS INJURY OR MEDICAL INTERVENTION REPORTED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7611427 ↗
  • InjuryDec 5, 2017Patient-Device Incompatibility

    IT WAS REPORTED THAT BD VACUTAINER® STRETCH LATEX FREE TOURNIQUET CAUSED ALLERGIC REACTIONS IN TWO PEOPLE. ONE REPORTED CONGESTION, HEADACHE, COUGH AND RESPIRATORY ISSUES. THE OTHER HAD DERMATITIS AND HIVES. BOTH WERE REASSIGNED TO WORK IN ANOTHER AREA. NO MEDICAL INTERVENTION REPORTED FOR THE REACTIONS.

    Patient problems: Headache; Hypersensitivity/Allergic reaction; Reaction; Skin Irritation

    MAUDE report 7082710 ↗

Other TOURNIQUET, NONPNEUMATIC devices

All TOURNIQUET, NONPNEUMATIC devices →

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