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Tamper Evident Cap 418004Recalls & reported problems

B. Braun Medical Inc. · Tamper Evident Syringe Cap - Red · Class 2

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

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04046963579678), received between Apr 17, 2023 and Apr 17, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (3 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.

Most reported problems

Device problems

  • Contamination /Decontamination Problem3

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

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

  • MalfunctionApr 17, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY. EVENT 2: THE TRANSPARENT CAPS HAVE WHITE RESIDUE INSIDE. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16751424 ↗
  • MalfunctionApr 17, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY. EVENT 3: THE TRANSPARENT CAPS HAVE WHITE RESIDUE INSIDE. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16751423 ↗
  • MalfunctionApr 17, 2023Contamination /Decontamination Problem; Contamination /Decontamination Problem

    AS REPORTED BY THE USER FACILITY: EVENT 1: THE TRANSPARENT CAPS HAVE WHITE RESIDUE INSIDE. NO INJURY REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16751422 ↗

Other Syringe, piston devices

All Syringe, piston devices →

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