FDA Adverse Event Other Summary report: N

KINAIR III WITH SCALE

MDR report key: 552584 · Received September 16, 2004

Report

Report Number
552584
Event Type
Other
Date Received
September 16, 2004
Date of Event
September 7, 2004
Report Date
September 16, 2004
Manufacturer
KINETIC CONCEPTS, INC
Product Code
IOQ
Report Source
User Facility report
Reporter Location
MN, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

OBESE PATIENT WITH SKIN BREAKDOWN ISSUES USING KINAIR III SPECIALTY BED WITH A SHEET APPLIED DIRECTLY OVER THE MATTRESS. GETTING OUT OF BED WAS A NEW ACTIVITY FOR PATIENT AS HAD BEEN ON BEDREST PRIOR TO THIS FALL. PRIOR TO THE FALL, THE BOTH OF THE BED'S SIDERAILS WERE UP AND THE HEAD OF THE BED WAS NOT UP TOO HIGH. NURSE HEARD PATIENT YELL OUT FOR HELP. PATIENT WAS ALERT, BUT FORGETFUL AND DID NOT USE NURSE CALL BUTTON APPROPRIATELY. STAFF IMMEDIATELY RESPONDED AND FOUND PATIENT SITTING ON THE FLOOR RIGHT NEXT TO THE BED. PATIENT REPORTED JUST SLIDING OFF OF THE BED PAST THE SIDE RAILS AND ONTO THE FLOOR. NURSE STAFF INDICATED THAT THE MATTRESS ON THIS BED IS SLIPPERY ESPECIALLY WITH A SHEET. IN THIS OCCURRENCE, THE HEAD OF THE BED WAS NOT UP THAT HIGH, BUT SOMETIMES WHEN THE HEAD OF THE BED IS UP HIGH, PATIENTS SLIDE MORE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 KINAIR III WITH SCALE BED, FLOATATION IOQ KINETIC CONCEPTS, INC KINAIR III WITH SCALE *

Patients

Seq Age Sex Outcome Treatment
1 73 YR OTHER