FDA Adverse Event Injury Summary report: N

35A MOBILE TRANSPORTER

MDR report key: 4336266 · Received December 4, 2014

Report

Report Number
1523574-2014-00022
Event Type
Injury
Date Received
December 4, 2014
Date of Event
July 29, 2014
Report Date
December 3, 2014
Manufacturer
FERNO-WASHINGTON, INC.
Product Code
FPO
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE SUBJECT UNIT WAS INSPECTED BY (B)(4) ON (B)(6) 2014. NO MALFUNCTIONS WERE DETECTED AND THE INCIDENT COULD NOT BE DUPLICATED. THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE DETERMINED.

Description of Event or Problem · 1

CUSTOMER ADVISED (B)(4) ON (B)(6) 2014 THAT WHILE LOADING A PATIENT INTO THE AMBULANCE THE STRETCHER LOWERED FROM THE CURRENT POSITION. THIS RESULTED IN A REPORTED INJURY TO THE PARAMEDIC. DETAILS OF THE INJURY OR ANY MEDICAL INTERVENTION WERE NOT DISCLOSED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
783000 35A MOBILE TRANSPORTER 35A MOBILE TRANSPORTER FPO FERNO-WASHINGTON, INC. 0015610

Patients

Seq Age Sex Outcome Treatment
1 Other