FDA Adverse Event Other Summary report: N

LD304 MATERNITY BED

MDR report key: 1911522 · Received November 22, 2010

Report

Report Number
1831750-2010-04050
Event Type
Other
Date Received
November 22, 2010
Date of Event
October 26, 2010
Report Date
October 26, 2010
Manufacturer
STRYKER CORP., MED DIV.
Product Code
HDD
PMA / PMN Number
K950889
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NZ
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT A MIDWIFE FROM (B)(6) TO ADVISE ON SHOULDER/NECK INJURY WHILE LIFTING A (B)(6) WOMAN'S LEGS ONTO THE STIRRUPS ON THE 4701 MATERNITY BED. THE BED WAS FOUND TO BE WORKING TO SPECIFICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LD304 MATERNITY BED LABOR AND DELIVERY BED HDD STRYKER CORP., MED DIV. 4701 NA

Patients

Seq Age Sex Outcome Treatment
1