FDA Adverse Event Injury Summary report: N

CONSERVE(R) TOTAL A-CLASS HEAD

MDR report key: 5068462 · Received September 10, 2015

Report

Report Number
3010536692-2015-01690
Event Type
Injury
Date Received
September 10, 2015
Date of Event
December 26, 2014
Report Date
September 9, 2015
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
JDL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS IS THE SAME EVENT AS 3010536692-2015-01689.

Description of Event or Problem · 1

ALLEGEDLY, PATIENT WAS REVISED DUE TO MOM COMPLICATIONS: PAIN; LOSS OF MOBILITY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
598712 CONSERVE(R) TOTAL A-CLASS HEAD HIP COMPONENT JDL MICROPORT ORTHOPEDICS INC. 08526122810

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention