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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ADVANTA 2 BED; NONE

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ADVANTA 2 BED; NONE Back to Search Results
Model Number 1190
Device Problem Device Inoperable (1663)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 05/15/2015
Event Type  malfunction  
Event Description
Hill-rom received a report from the account stating the nurse call would not work.The bed was located at the account.There was no patient/user injury reported.This report was filed in our complaint handling system as complaint #(b)(4).
 
Manufacturer Narrative
The hill-rom tech found the nurse call cable and pendant had failed.A search of the hill-rom maintenance records did not show hill-rom performed preventative maintenance on this bed.It is unknown if the facility performs preventative maintenance on their beds.The tech replaced the cable and pendant to resolve the issue.Based on this information, no further action is required.
 
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Brand Name
ADVANTA 2 BED
Type of Device
NONE
Manufacturer Contact
tony werner
1069 state rte 46 e
batesville, IN 47006
8129312359
MDR Report Key4848185
MDR Text Key5805639
Report Number3006697241-2015-00258
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 05/15/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/09/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model Number1190
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Date Manufacturer Received05/15/2015
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured03/01/2010
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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