FDA Adverse Event Malfunction Summary report: N

LD304 MATERNITY BED

MDR report key: 2960978 · Received February 14, 2013

Report

Report Number
0001831750-2013-01132
Event Type
Malfunction
Date Received
February 14, 2013
Date of Event
January 21, 2013
Report Date
January 22, 2013
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
HDD
PMA / PMN Number
K950889
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: LOAD CELL.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE WAS INACCURATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
64362 LD304 MATERNITY BED TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES) HDD STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1