FDA Adverse Event Other Summary report: N

TOTALCARE

MDR report key: 1736340 · Received June 22, 2010

Report

Report Number
1824206-2010-08400
Event Type
Other
Date Received
June 22, 2010
Date of Event
March 22, 2010
Report Date
May 26, 2010
Manufacturer
HILL-ROM, INC.
Product Code
FNL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN ASSISTED THE STAFF TO MOVE A (B)(6) PT UP IN BED AND OBSERVED THAT THE TOPPER MOVED UP WITH PT AND THE PT DID NOT SLIDE UP IN BED. THE ACCOUNT REQUESTED A DARTEX STYLE TICKING AS THEY BELIEVE IT IS EASIER TO MOVE THE PT ON IT.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES CAREGIVERS ARE INJURING THEIR BACKS DUE TO PATIENTS BEING DIFFICULT TO MOVE ON THE MATTRESS TICKING. THE NURSE ALLEGED THAT SHE WAS ASSISTING ANOTHER NURSE TO REPOSITION A PT AND THE MATTRESS DID NOT ALLOW THE PT TO SLIDE UP IN BED. WITH THE MATTRESS IN MAX INFLATE AND A SHEET AND PAD ON THE BED, THE PT "STICKS" TO THE MATTRESS MAKING IT DIFFICULT TO SLIDE THE PT. THE HOSPITAL WOULD NOT RELEASE ANY INFORMATION REGARDING THE ALLEGED INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM, INC. 1916

Patients

Seq Age Sex Outcome Treatment
1 UNK