FDA Adverse Event Injury Summary report: N

CONSERVE® PLUS SPIKED CUP

MDR report key: 7527291 · Received May 18, 2018

Report

Report Number
3010536692-2018-00661
Event Type
Injury
Date Received
May 18, 2018
Report Date
May 18, 2018
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
HWT
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

ALLEGEDLY THE PATIENT WAS EXPERIENCING UNKNOWN MOM COMPLICATIONS. ADDITIONAL INFORMATION RECEIVED FROM LITIGATIONS ON 05/09/2018. ALLEGEDLY THE PATIENT WAS REVISED DUE TO MOM COMPLICATIONS. (LEFT).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
368800 CONSERVE® PLUS SPIKED CUP HIP COMPONENT HWT MICROPORT ORTHOPEDICS INC. NI

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention