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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HILL-ROM, INC. RPOGRESSA BED; A/C POWERED ADJUSTABLE HOSPITAL BED
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HILL-ROM, INC. RPOGRESSA BED; A/C POWERED ADJUSTABLE HOSPITAL BED Back to Search Results
Model Number 7500
Device Problem Positioning Problem (3009)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 05/08/2015
Event Type  malfunction  
Event Description
Hill-rom received a report from the account stating the intellidrive was running in reverse when pushing forward.The bed was located at the account.There was no patient/user injury reported.(b)(4).
 
Manufacturer Narrative
The technician found the left hand push handle was the issue.A search of the hill-rom maintenance records did not show hill-rom performed any preventative maintenance on this bed.It is unknown if the facility performs preventative maintenance on their beds.The technician replaced the left hand push handle to resolve the issue.Based on this information, no further action is required.
 
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Brand Name
RPOGRESSA BED
Type of Device
A/C POWERED ADJUSTABLE HOSPITAL BED
Manufacturer (Section D)
HILL-ROM, INC.
batesville IN
Manufacturer Contact
tony werner
1069 state route 46 east
batesville, IN 47006
8129312359
MDR Report Key4843924
MDR Text Key5937170
Report Number1824206-2015-00632
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,Company Representative
Reporter Occupation Unknown
Type of Report Initial
Report Date 05/08/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model Number7500
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 05/08/2015
Initial Date FDA Received06/03/2015
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured04/01/2014
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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