FDA Adverse Event Death Summary report: N

SYNVISC

MDR report key: 16478286 · Received March 2, 2023

Report

Report Number
MW5115407
Event Type
Death
Date Received
March 2, 2023
Date of Event
February 27, 2023
Report Date
February 28, 2023
Manufacturer
GENZYME CORPORATION
Product Code
MOZ
UDI-DI
58468009003
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
AR, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND
Health Professional
N

Narratives

Description of Event or Problem · 0

PT'S WIFE REPORTED THAT (B)(6) WAS DECEASED ON (B)(6) 2023, THE CAUSE OF DEATH WAS NOT PROVIDED BY THE REPORTER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1871476 SYNVISC ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION 58468009003

Patients

Seq Age Sex Outcome Treatment
1 88 YR Male Death