FDA Adverse Event Injury Summary report: N

UNKNOWN MAESTRO WRIST

MDR report key: 6204740 · Received December 27, 2016

Report

Report Number
0001825034-2016-05292
Event Type
Injury
Date Received
December 27, 2016
Report Date
December 27, 2016
Manufacturer
BIOMET ORTHOPEDICS
Product Code
JWJ
PMA / PMN Number
PNI
Removal / Correction Number
NI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

MICHAEL P. GASPER- "COMPLICATIONS FOLLOWING PARTIAL AND TOTAL WRIST ARTHROPLASTY" 1-11. THE PRODUCT IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY WAS NOT PROVIDED. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. INITIAL REPORTER - JESSE LOU, PATRICK M. KANE, SIDNEY M. JACOBY, A. LEE OSTERMAN, AND RANDALL W. CULP.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT THREE PATIENTS INITIALLY UNDERWENT DISTAL RADIUS HEMIARTHOPLASTY. POST OPERATIVELY PATIENTS INDICATED NERVE COMPRESSION IN CT OR GUYAN CANAL SYNDROME. THERE HAS BEEN NO FURTHER INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
857284 UNKNOWN MAESTRO WRIST PROSTHESIS, WRIST JWJ BIOMET ORTHOPEDICS NI NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R