FDA Adverse Event Death Summary report: N

UNKNOWN HIP SYSTEM

MDR report key: 24185279 · Received January 26, 2026

Report

Report Number
3010536692-2024-00487
Event Type
Death
Date Received
January 26, 2026
Report Date
September 2, 2025
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
LZO
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS EVENT WILL BE UPDATED ONCE THE INVESTIGATION IS COMPLETE. TRENDS WILL BE EVALUATED.

Description of Event or Problem · 0

ALLEGEDLY, 2 WEEKS POST SUPERPATH MICROPORT HIP REPLACEMENT, THE SURGERY HIP/LEG IS LONGER THAN THE OTHER LEG, LIMP DUE TO THE LEG DISCREPANCY.

Description of Event or Problem · 0

ALLEGEDLY, 2 WEEKS POST SUPERPATH MICROPORT HIP REPLACEMENT, THE SURGERY HIP/LEG IS LONGER THAN THE OTHER LEG, LIMP DUE TO THE LEG DISCREPANCY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
242431 UNKNOWN HIP SYSTEM HIP COMPONENT LZO MICROPORT ORTHOPEDICS INC. XXXXXXXX NI

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention