Skip to content

NA 4437Recalls & reported problems

Carefusion 2200, Inc · Dry Gauze Preoperative Skin Prep Tray With Powder-Free Gloves · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403175213), received between Feb 4, 2021 and Feb 4, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Contamination /Decontamination Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 4, 2021Contamination /Decontamination Problem; Contamination /Decontamination Problem

    IT WAS REPORTED THAT CUSTOMER FOUND A BUG ON THE PACKAGING.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Known Impact Or Consequence To Patient

    MAUDE report 11278801 ↗

Other Skin prep tray devices

All Skin prep tray devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page