FDA Adverse Event Malfunction Summary report: N

LD304 MATERNITY BED

MDR report key: 2800267 · Received October 8, 2012

Report

Report Number
1831750-2012-10502
Event Type
Malfunction
Date Received
October 8, 2012
Date of Event
September 10, 2012
Report Date
September 10, 2012
Manufacturer
STRYKER MEDICAL
Product Code
HDD
PMA / PMN Number
K950889
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

HEAD END LITTER COVER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD END LITTER COVER WAS BROKEN, EXPOSING SHARP EDGES. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LD304 MATERNITY BED LABOR AND DELIVERY BED HDD STRYKER MEDICAL 4701 NA

Patients

Seq Age Sex Outcome Treatment
1