FDA Adverse Event Death Summary report: N

EUFLEXXA PFS 20MG/2ML

MDR report key: 23311698 · Received October 16, 2025

Report

Report Number
MW5177444
Event Type
Death
Date Received
October 16, 2025
Date of Event
September 29, 2025
Report Date
October 14, 2025
Manufacturer
FERRING PHARMACEUTICALS INC.
Product Code
MOZ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND
Health Professional
*

Narratives

Description of Event or Problem · 0

THE CAUSE OF DEATH WAS NOT PROVIDED BY THE REPORTER. PRESCRIBER NAME: (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2665476 EUFLEXXA PFS 20MG/2ML ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC.

Patients

Seq Age Sex Outcome Treatment
1 97 YR Unknown Death