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Medline Industries, Inc. DYNJ0744881IRecalls & reported problems

Medline Industries, Inc. · ROBOTIC PACK · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10193489943245), received between Oct 27, 2021 and Oct 27, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

  • Detachment of Device or Device Component1

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.

  • InjuryOct 27, 2021Detachment of Device or Device Component

    IT WAS REPORTED THAT IN THE MIDDLE OF THE PROCEDURE PIECES OF STRING WERE DISCOVERED INSIDE THE PATIENT'S SURGICAL SITE FROM THE GAUZE SPONGE.

    Patient problems: Foreign Body In Patient

    MAUDE report 12706343 ↗

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Sources and updates

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