FDA Adverse Event Malfunction Summary report: N

TRAUMA STRETCHER

MDR report key: 3130454 · Received March 26, 2013

Report

Report Number
3006697241-2013-00066
Event Type
Malfunction
Date Received
March 26, 2013
Manufacturer
HILLROM DE MEXICO S DE RL DE CV
Product Code
FPO
Report Source
Manufacturer report

Narratives

Additional Manufacturer Narrative · 1

THE ACCOUNT ADJUSTED ALL BRAKE CASTERS TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

REF IMP REPORT: (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
125407 TRAUMA STRETCHER WHEELED STRETCHER FPO HILLROM DE MEXICO S DE RL DE CV

Patients

Seq Age Sex Outcome Treatment
1