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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HILL-ROM, INC. ADVANTA BED; A/C POWERED ADJUSTABLE HOSP BED
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HILL-ROM, INC. ADVANTA BED; A/C POWERED ADJUSTABLE HOSP BED Back to Search Results
Model Number 1604
Device Problem Sticking (1597)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 05/05/2014
Event Type  malfunction  
Event Description
Hill-rom received a report from the account stating the left foot siderail would not latch.The bed was located at the account in the hca warehouse.There was no pt/user injury reported.(b)(4).
 
Manufacturer Narrative
The hill-rom technician found the siderail not latching due to the release arm being stuck.A search of the hill-rom maintenance records showed hill-rom performed preventative maintenance on this bed in 2013.It is unk if the facility performed any other preventative maintenance on this bed.The tech lubricated the release arm to resolve the issue.Based on this info, no further action is required.
 
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Brand Name
ADVANTA BED
Type of Device
A/C POWERED ADJUSTABLE HOSP BED
Manufacturer (Section D)
HILL-ROM, INC.
batesville IN
Manufacturer Contact
john cummings
1069 state route 46 e
batesville, IN 47006
8129312869
MDR Report Key3880836
MDR Text Key20972811
Report Number1824206-2014-01658
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 User Facility
Reporter Occupation Unknown
Type of Report Initial
Report Date 05/05/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/29/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model Number1604
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Date Manufacturer Received05/05/2014
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured02/01/2002
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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