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 |