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Lineage 20070053Recalls & reported problems

Microport Orthopedics Inc. · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI M684200700531), received between Sep 26, 2019 and Sep 26, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (2 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information2

Patient problems

  • No Information2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjurySep 26, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, UNIVERSAL HANDLE: BREAKING OF THE TEETH CONJUNCTION BROACH TIP ZELPI RETRACTORS: THE SELF RETAINING TEETH DOESN'T KEEP THE POSITION ROUND CALCARS: BREAKING OF THE CONJUNCTION FILLET. SURGERY WAS EXTENDED GREATER THAN 30 MINUTES.

    Patient problems: No Information

    MAUDE report 9126012 ↗
  • InjurySep 26, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY, UNIVERSAL HANDLE: BREAKING OF THE TEETH CONJUNCTION BROACH TIP. ZELPI RETRACTORS: THE SELF RETAINING TEETH DOESN'T KEEP THE POSITION. ROUND CALCARS: BREAKING OF THE CONJUNCTION FILLET. SURGERY WAS EXTENDED GREATER THAN 30 MINUTES.

    Patient problems: No Information

    MAUDE report 9126011 ↗

Other PUNCH, FEMORAL NECK devices

All PUNCH, FEMORAL NECK devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.