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Anthology 71365600Recalls & reported problems

Smith & Nephew, Inc. · ANTHOLOGY STARTER BROACH · Class 2

All models of ANTHOLOGY (69)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 03596010559807), received between Jun 30, 2019 and Nov 30, 2020 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (3 reports).

2 other recalls cover devices cleared under the same FDA submission (K123598); they may or may not involve this specific model.

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

  • Inadequacy of Device Shape and/or Size3
  • Connection Problem1
  • Dull, Blunt1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 30, 2020Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

    IT WAS REPORTED THAT SIZING ISSUES WITH THE ANTHOLOGY CASE WERE NOTICED. IT WAS NOT POSSIBLE TO ATTRIBUTE THE ISSUE TO ANY PARTICULAR INSTRUMENT AND THERE IS NO SINGULAR SURGERY TO CITE. NO FURTHER INFORMATION REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10920538 ↗
  • MalfunctionNov 30, 2020Inadequacy of Device Shape and/or Size; Dull, Blunt; Inadequacy of Device Shape and/or Size; Dull, Blunt

    IT WAS REPORTED THAT SIZING ISSUES WITH THE ANTHOLOGY CASE WERE NOTICED. IT WAS NOT POSSIBLE TO ATTRIBUTE THE ISSUE TO ANY PARTICULAR INSTRUMENT AND THERE IS NO SINGULAR SURGERY TO CITE. NO FURTHER INFORMATION REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10920264 ↗
  • MalfunctionNov 30, 2020Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

    IT WAS REPORTED THAT SIZING ISSUES WITH THE ANTHOLOGY CASE WERE NOTICED. IT WAS NOT POSSIBLE TO ATTRIBUTE THE ISSUE TO ANY PARTICULAR INSTRUMENT AND THERE IS NO SINGULAR SURGERY TO CITE. NO FURTHER INFORMATION REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10919962 ↗
  • MalfunctionJun 30, 2019Connection Problem; Connection Problem

    IT WAS REPORTED THAT DURING PROCEDURE HAD TROUBLES WITH THE BROACHES ARE THEY WERE NOT RELEASING FROM THE HANDLE. THE SCRUB NURSES NOTICED THAT THEY WERE NOT EASILY ATTACHING AND DETACHING.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8746825 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K123598. One submission often covers many models, so check the product and lot details in each record.

  • Z-0730-2019 · Jan 7, 2019 · Terminated
    SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
  • Z-1008-2017 · Nov 16, 2016 · Terminated
    REFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,. Memphis, TN 38116

Other Prosthesis, hip, femoral component, cemented, metal devices

All Prosthesis, hip, femoral component, cemented, metal devices →

Sources and updates

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