InjuryLWJ
AESCULAP
Received Jul 7, 2026
Report 3005673311-2026-00138 · MDR key 25734525
Device
Generic name
Prosthesis, Hip, Semi-constrained, Metal/polymer, Uncemented
Manufacturer
Aesculap AgModel number
NH413Catalog number
NH413
Product problems
- Fracture
Patient
NA · Male
- Insufficient Information
Narrative
Description of Event or Problem
AN ADVERSE EVENT WAS REPORTED INVOLVING THE AESCULAP KNEE IMPLANTS. SPECIFICALLY IT WAS REPORTED THAT FOLLOWING HIP SURGERY IN 2017, THE PATIENT EXPERIENCED A FALL. SUBSEQUENT EVALUATION REPORTEDLY IDENTIFIED A FRACTURE OF THE IMPLANTED MEDICAL DEVICE. REVISION SURGERY IS REQUIRED. THE SURGERY WAS PERFORMED IN ARGENTINA, AT HOSPITAL PRIVADO DE CÓRDOBA, BUT THE PATIENT CURRENTLY LIVES AND IS IN MIAMI. THIS REPORT IS FILED UNDER AIS REFERENCE (B)(4). .