FDA Adverse Event Injury Summary report: N

RIM-LOCK

MDR report key: 10363239 · Received August 4, 2020

Report

Report Number
3010536692-2020-00553
Event Type
Injury
Date Received
August 4, 2020
Date of Event
August 29, 2013
Report Date
August 4, 2020
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
LPH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
DE
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

ALLEGEDLY, WOUND INFECTION IN THE PATIENT RIGHT HIP WAS DETECTED. THE PATIENT HAD A MEDICAL INTERVENTION FOR WOUND DEBRIDEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
824787 RIM-LOCK HIP COMPONENT LPH MICROPORT ORTHOPEDICS INC. PHA04658 1494324

Patients

Seq Age Sex Outcome Treatment
1 68 YR Required Intervention