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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HILL-ROM, INC. CENTURY BED; A/C POWERED ADJUSTABLE HOSPITAL BED
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HILL-ROM, INC. CENTURY BED; A/C POWERED ADJUSTABLE HOSPITAL BED Back to Search Results
Model Number 835
Device Problem Sticking (1597)
Patient Problem Physical Entrapment (2327)
Event Date 02/25/2014
Event Type  malfunction  
Event Description
Hill-rom received a report from a hill-rom technician stating the release arm was stuck against side rail support arm and the latch block was not moving.The bed was located at the account in the bed shop.There was no pt/user injury reported.(b)(4).
 
Manufacturer Narrative
The hill-rom technician found the siderail would not latch.Per the hill-rom service manual the century bed requires an effective maintenance program.We recommend that you perform annual preventative maintenance.Check the side rail and ensure that it latches properly.Adjust if necessary.A search of the hill-rom maintenance records showed hill-rom performed preventative maintenance on this bed in 2006-2012 and 2014.It is unk if the facility performs any other preventative maintenance on this bed.The technician adjusted the release arm into correct position to resolve the issue.Based on this info, no further action is required.
 
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Brand Name
CENTURY BED
Type of Device
A/C POWERED ADJUSTABLE HOSPITAL BED
Manufacturer (Section D)
HILL-ROM, INC.
batesville IN
Manufacturer Contact
john cummings
1069 state route 46 east
batesville, IN 47006
8129312869
MDR Report Key3783373
MDR Text Key4430774
Report Number1824206-2014-00962
Device Sequence Number1
Product Code FNL
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 02/25/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/24/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model Number835
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Date Manufacturer Received02/25/2014
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured06/01/1985
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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