Skip to content

Multifire Endo GIA 030331Recalls & reported problems

Covidien LP · Straight Stapler · Class 2 · Implant

All models of Multifire Endo GIA (5)

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 10884523003741), received between Dec 17, 2019 and Dec 17, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Cut” (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

  • Failure to Cut1

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.

  • MalfunctionDec 17, 2019Failure to Cut; Failure to Cut

    ACCORDING TO THE REPORTER, INTRA-OPERATIVELY, ONE RELOAD DID NOT DEPLOY STAPLES AND THE OTHER RELOAD ONLY DEPLOYED THE PROXIMAL END OF STAPLES. IT WAS ALSO STATED THAT ONE HANDLE DEPLOYED THE STAPLES BUT DID NOT CUT. THERE WAS NO PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9480424 ↗

Other STAPLE, IMPLANTABLE devices

All STAPLE, IMPLANTABLE devices →

Sources and updates

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