FDA Adverse Event
Other
Summary report: N
GUARDIAN WALKER
MDR report key: 412190
·
Received August 22, 2002
Report
- Report Number
- 2020334-2002-00007
- Event Type
- Other
- Date Received
- August 22, 2002
- Report Date
- August 22, 2002
- Manufacturer
- SUNRISE MEDICAL/PCP DIVISION
- Product Code
- ITJ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT THE END USER WAS USING THE WALKER AT HOME, WHEN THE WALKER COLLAPSED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GUARDIAN WALKER | PATIENT WALKER | ITJ | SUNRISE MEDICAL/PCP DIVISION | 30755P | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 74 YR | Hospitalization| O |