FDA Adverse Event Other Summary report: N

HOSPITAL BED

MDR report key: 2031893 · Received March 21, 2011

Report

Report Number
2182305-2011-00007
Event Type
Other
Date Received
March 21, 2011
Date of Event
February 23, 2011
Report Date
March 17, 2011
Manufacturer
JOERNS HEALTHCARE
Product Code
FNL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED TO MFR, BY FACILITY; (B)(6), PER FACILITY THEY HAD A BED CENTER PIVOT BRACKET COME LOOSE AND THE BED ALLEGEDLY DROPPED, CAUSING THE RESIDENT MINOR INJURY OF BACK PAIN AND SOME BRUISING. THIS WAS PART OF AN EARLY ORDER OF 170 BEDS THAT THE PIVOT BRACKETS WERE COMING LOOSE FROM THE MAIN FRAME WHICH THE FACILITY REQUESTED A FEW BRACKETS KITS AT THAT TIME; THEY ARE REQUESTING 6 MORE BRACKET KITS. (B)(4) ENTERED NO RA WAS ISSUED TO GET PARTS BACK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HOSPITAL BED HOSPITAL BED MANUAL FNL JOERNS HEALTHCARE B330

Patients

Seq Age Sex Outcome Treatment
1 UNK Other