FDA Adverse Event Malfunction Summary report: N

RENAISSANCE 29 P-WASHOBS

MDR report key: 2160654 · Received June 30, 2011

Report

Report Number
1831750-2011-06685
Event Type
Malfunction
Date Received
June 30, 2011
Date of Event
June 3, 2011
Report Date
June 3, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

CONCLUSION: THE PART HAS BEEN ORDERED AND THE SVC TECH WILL RETURN TO COMPLETE THE REPAIR.

Description of Event or Problem · 1

IT WAS REPORTED BY SVC REPORT THAT THE STRETCHER DRIFTS DOWN. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RENAISSANCE 29 P-WASHOBS WHEELED STRETCHER FPO STRYKER MEDICAL 1731 NA

Patients

Seq Age Sex Outcome Treatment
1