Accord 71340011Recalls & reported problems
Smith & Nephew, Inc. · ACCORD STANDARD 125MM 5 CABLE TROCHANTERIC GRIP · Class 2 · Implant
All models of Accord (14)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 03596010485809), received between Aug 23, 2018 and Feb 11, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (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
- Break1
- Disconnection1
Patient problems
- Failure of Implant1
- No Code Available1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 11, 2019Break; Break
IT WAS REPORTED THAT PATIENT WHO HAD INTERTAN OPERATION ON (B)(6) 2017 AT THIS HOSPITAL HAD PAIN AND TOOK X-RAY AT OTHER HOSPITAL, THEN IT WAS NOTED THAT THE NAIL WAS BROKEN. REVISION SURGERY (BHR) WIL BE PERFORMED.
Patient problems: Pain
MAUDE report 8329903 ↗InjuryAug 23, 2018Disconnection
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED DUE TO THE PATIENT'S TROCHANTERIC REGION AND GREATER TROCHANTER WAS COMPLETELY UNUNITED. THE CABLES AND CLAW WERE REMOVED. THE TROCHANTERIC NONUNION WAS FIXED BY REAPPROXIMATING THE GREATER TROCHANTER IN THE APPROPRIATE POSITION AND PLACING A NEW CABLE CLAW CONSTRUCT IN THE APPROPRIATE POSITION.
Patient problems: Failure of Implant; No Code Available
MAUDE report 7808613 ↗
Other CERCLAGE, FIXATION devices
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- CONTROL 1739-28-000Depuy Orthopaedics, Inc. · CERCLAGE, FIXATION52 reports
- Dall-Miles 6704-0-110Howmedica Osteonics Corp. · CERCLAGE, FIXATION1 recall1 report
- Tritium® Sternal Cable Plate System 86-27-12-S12Pioneer Surgical Technology, Inc. · CERCLAGE, FIXATION1 recall0 reports
- Accord 71340007Smith & Nephew, Inc. · CERCLAGE, FIXATION47 reports
- ZipFix 08.501.001.01SSynthes GmbH · CERCLAGE, FIXATION39 reports
- NA 298.801.01SSynthes GmbH · CERCLAGE, FIXATION33 reports
- ZipFix 08.501.001.05SSynthes GmbH · CERCLAGE, FIXATION29 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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