FDA Adverse Event
Death
Summary report: N
SYNVISC ONE PFS 8MG/ML
MDR report key: 23922171
·
Received December 30, 2025
Report
- Report Number
- MW5181421
- Event Type
- Death
- Date Received
- December 30, 2025
- Report Date
- December 22, 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
(B)(6), WIFE REPORTING PT IS PASSED AWAY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1768851 | SYNVISC ONE PFS 8MG/ML | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 99 YR | Male | Death |