FDA Adverse Event
Death
Summary report: N
SYNVISC ONE PFS 8MG/ML
MDR report key: 17877359
·
Received October 4, 2023
Report
- Report Number
- MW5146606
- Event Type
- Death
- Date Received
- October 4, 2023
- Report Date
- September 29, 2023
- Manufacturer
- GENZYME CORPORATION
- Product Code
- MOZ
- UDI-DI
- 58468009003
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
PATIENT DECEASED. (B)(6).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 225951 | SYNVISC ONE PFS 8MG/ML | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION | 58468009003 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Female | Death |