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Medline Industries, Inc. DYNJS3071Recalls & reported problems

Medline Industries, Inc. · KP SINGLE BASIN SURE SET RF · Class 2

Data updated Oct 18, 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 10888277248908), received between Sep 3, 2019 and Sep 3, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Fragmentation” (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 18, 2026.

Most reported problems

Device problems

  • Material Fragmentation1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • MalfunctionSep 3, 2019Material Fragmentation

    IT WAS REPORTED THAT THE GAUZE SHREDDED WHILE INSIDE OF A PATIENT.

    Patient problems: Foreign Body In Patient

    MAUDE report 8957115 ↗

Other General surgery tray devices

All General surgery tray devices →

Sources and updates

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