FDA Adverse Event Other Summary report: N

SECURE II MED/SURG BED

MDR report key: 1790572 · Received August 2, 2010

Report

Report Number
1831750-2010-01687
Event Type
Other
Date Received
August 2, 2010
Date of Event
July 8, 2010
Report Date
July 8, 2010
Manufacturer
STRYKER CORP, MEDICAL DIV
Product Code
FNL
Removal / Correction Number
UNK
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CONCLUSION: INVESTIGATION IS ONGOING TO PROVIDE CONCLUSIONS.

Description of Event or Problem · 1

IT WAS REPORTED THAT, THE FACILITY HAD A CAREGIVER INJURY AS A RESULT OF THE BRAKES NOT HOLDING PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE II MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP, MEDICAL DIV 3002 NA

Patients

Seq Age Sex Outcome Treatment
1 NA Other