FDA Adverse Event
Death
Summary report: N
SYNVISC ONE
MDR report key: 23888119
·
Received December 24, 2025
Report
- Report Number
- MW5181163
- Event Type
- Death
- Date Received
- December 24, 2025
- Report Date
- December 19, 2025
- Manufacturer
- GENZYME CORPORATION
- 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
PATIENT'S DAUGHTER (B)(6) REPORTED PATIENT DIED ON (B)(6) 2025. CAUSE OF THE DEATH IS NOT REPORTED BY THE PROVIDER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2531695 | SYNVISC ONE | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 83 YR | Female | Death |