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CHS 121142Recalls & reported problems

Smith & Nephew, Inc. · AMBI COMPRESSION HIP SCREW PLATE 6SL 140MM 140D · Class 2 · Implant

All models of CHS (30)

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010062154), received between Mar 10, 2021 and Mar 10, 2021 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Metal Related Pathology1
  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 10, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT, AFTER BHR IMPLANT SURGERY PERFORMED IN (B)(6) 2003, DUE TO SEVERE PAIN, A REVISION SURGERY WAS PERFORMED IN (B)(6) 2011, THERE IS A DIAGNOSIS FOR METALLOSIS, AND THERE IS STILL A LOT OF PAIN, AND RESPIRATORY ISSUES REPORTED, PATIENT IS WAITING FOR ANOTHER SURGERY.

    Patient problems: Metal Related Pathology; Pain

    MAUDE report 11456807 ↗

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices

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Sources and updates

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