Cable-Ready® 2232-03-02Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
All models of Cable-Ready (10)
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 00889024039476), received between Apr 18, 2024 and Apr 18, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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.
Reports received per month
Most reported problems
Device problems
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- Numbness1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 18, 2024Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
IT WAS REPORTED THAT A PATIENT UNDERWENT AN INITIAL TOTAL HIP ARTHROPLASTY APPROXIMATELY ELEVEN (11) YEARS AGO AND AN OPEN REDUCTION INTERNAL FIXATION DUE TO PERIPROSTHETIC FRACTURE APPROXIMATELY TWO (2) YEARS AND SIX (6) MONTHS AFTER THE PATIENT'S INITIAL SURGERY. SUBSEQUENTLY, THE PATIENT WAS EXPERIENCING PAIN, NUMBNESS, AND LEFT SIDED SCIATICA AND UNDERWENT A REVISION SURGERY APPROXIMATELY ONE (1) MONTH AGO. DURING THE REVISION IT WAS DISCOVERED THAT THE FEMORAL STEM HAD LOOSENED. THERE WAS NO PRESENCE OF AN INFECTION. ALL OF THE FEMORAL COMPONENTS AND PLATES WERE REVISED. THE ACETABULAR COMPONENTS WERE LEFT IMPLANTED IN THE PATIENT.
Patient problems: Numbness; Pain
MAUDE report 19136256 ↗
Other CERCLAGE, FIXATION devices
- ZipFix 03.501.080Synthes GmbH · CERCLAGE, FIXATION236 reports
- 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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