MAUDE Adverse Event Report: GENZYME CORPORATION SYNVISC PFS 8 MG/ML (3X2 ML); ACID, HYALURONIC, INTRAARTICULAR

Patient Problem Insufficient Information (4580)

Event Type  Death  

Event Description

Pt is deceased.The cause of death was not provided by the reporter.

• Brand Name: SYNVISC PFS 8 MG/ML (3X2 ML)
• Type of Device: ACID, HYALURONIC, INTRAARTICULAR
• Manufacturer (Section D): GENZYME CORPORATION
• MDR Report Key: 18911877
• MDR Text Key: 337752598
• Report Number: MW5152861
• Device Sequence Number: 1
• Product Code: MOZ
• Combination Product (y/n): Y
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Unknown
• Type of Report: Initial
• Report Date: 03/12/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 03/14/2024
• Patient Sequence Number: 1
• Patient Outcome(s): Death
• Patient Age: 67 YR
• Patient Sex: Male