FDA Adverse Event
Injury
Summary report: N
SYNVISC
MDR report key: 10836781
·
Received November 12, 2020
Report
- Report Number
- MW5097842
- Event Type
- Injury
- Date Received
- November 12, 2020
- Date of Event
- March 21, 1999
- Report Date
- April 13, 1999
- Manufacturer
- GENZYME CORPORATION
- Product Code
- MOZ
- Report Source
- Voluntary report
- Reporter Location
- VA, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
SYNOVITIS OF (L) KNEE "JOINT RESULTS, AND REFERENCED HERE." BIOMATRIX..
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1298877 | SYNVISC | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 54 YR | Required Intervention |