FDA Adverse Event Death Summary report: N

SYNVISC ONE PFS 8MG/ML

MDR report key: 16529124 · Received March 10, 2023

Report

Report Number
MW5115647
Event Type
Death
Date Received
March 10, 2023
Report Date
March 8, 2023
Manufacturer
GENZYME CORPORATION
Product Code
MOZ
UDI-DI
58468009003
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
UNKNOWN
Health Professional
N

Narratives

Description of Event or Problem · 0

PT IS DECEASED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
445579 SYNVISC ONE PFS 8MG/ML ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION 58468009003

Patients

Seq Age Sex Outcome Treatment
1 Female Death