FDA Adverse Event Injury Summary report: N

*

MDR report key: 1080740 · Received June 13, 2008

Report

Report Number
1525712-2008-00047
Event Type
Injury
Date Received
June 13, 2008
Manufacturer
INVACARE CORP. - MANUFACTURING FACILITY
Product Code
FSA
Report Source
Manufacturer report
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * * FSA INVACARE CORP. - MANUFACTURING FACILITY * NA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention