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Medline Industries, Inc. DYNJ47688CRecalls & 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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942190089), received between Feb 7, 2019 and Feb 7, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Fell” (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

  • Device Fell1
  • Material Split, Cut or Torn1

Patient problems

  • No Consequences Or Impact 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 7, 2019Material Split, Cut or Torn; Device Fell

    IT WAS REPORTED THAT AS THE GAUZE COMPONENT WAS BEING REMOVED FROM THE SURGICAL SITE, DURING A ROBOTIC GASTROJEJUNOSTOMY PROCEDURE, IT RIPPED AND A PIECE FELL BACK INTO THE SURGICAL SITE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8317514 ↗

Other laparoscopy kit devices

All laparoscopy kit devices →

Sources and updates

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