Anthology 71365230KTRecalls & reported problems
Smith & Nephew, Inc. · ANTHOLOGY ANTERIOR BROACH HANDLE KIT · Class 1
All models of ANTHOLOGY (69)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00885556202845), received between Nov 26, 2020 and Nov 30, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Inadequacy of Device Shape and/or Size3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 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 10920148 ↗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 10919751 ↗MalfunctionNov 26, 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 10912552 ↗
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- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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