Skip to content

CHIMAERA Hip Fracture System 1 (REF 99-T932380L)Recalls & reported problems

Orthofix Srl · CHIMAERA HFS LONG NAIL LEFT 125° L380MM D11MM STERILE · Class 2 · Implant

All models of CHIMAERA Hip Fracture System (16)

Data updated Oct 18, 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 18054242514350), received between Jul 9, 2018 and Jul 9, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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 18, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryJul 9, 2018Fracture; Fracture

    THE INFORMATION PROVIDED BY THE LOCAL DISTRIBUTOR INDICATES: HOSPITAL NAME: (B)(6). SURGEON'S NAME: DR. (B)(6). DATE OF INITIAL SURGERY: (B)(6) 2018. BODY PART TO WHICH DEVICE WAS APPLIED: FEMUR PROXIMAL. SURGERY DESCRIPTION: FRACTURE TREATMENT. PATIENT INFORMATION: (B)(6), MALE, (B)(6), HEIGHT 175 CM, PREVIOUS HEALTH CONDITION: ASA III. EVENT DESCRIPTION: BREAKAGE OF THE CHIMAERA-NAIL 4 MONTHS AFTER OSTEOSYNTHESIS OF AN INTERTROCHANTERIC FRACTURE: REMOVAL OF THE CHIMAERA-NAIL AND HIP REPLACEMENT WITH A REVISION ENDOPROSTHESIS. THE COMPLAINT REPORT FORM ALSO INDICATES: THE DEVICE FAILURE HAD ADVERSE EFFECTS ON PATIENT. THE INITIAL SURGERY WAS COMPLETED WITH THE DEVICE. THE EVENT DID NOT LEAD TO A CLINICALLY RELEVANT INCREASE IN THE DURATION OF THE SURGICAL PROCEDURE. AN ADDITIONAL SURGERY WAS REQUIRED FOLLOWING DEVICE FAILURE: PERFORMED ON (B)(6) 2018. A MEDICAL INTERVENTION (OUTPATIENT CLINIC) WAS NOT REQUIRED. COPIES OF THE OPERATIVE REPORTS ARE NOT AVAILABLE. COPIES OF THE X-RAY IMAGES ARE AVAILABLE. FURTHER INFORMATION RECEIVED FROM THE DISTRIBUTOR: -RECEIVED COPY OF TWO PREOPERATIVE X-RAY IMAGES -RECEIVED COPY OF TWO POSTOPERATIVE X-RAY IMAGES: 1)POSTOPERATIVE, 2) AFTER FAILUR

    Patient problems: No Code Available

    MAUDE report 7669119 ↗

Other Rod, Fixation, Intramedullary And Accessories devices

All Rod, Fixation, Intramedullary And Accessories devices →

Sources and updates

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