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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ADVANCED BIONICS, LLC HIRES ULTRA 3D IMPLANT; COCHLEAR IMPLANT

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ADVANCED BIONICS, LLC HIRES ULTRA 3D IMPLANT; COCHLEAR IMPLANT Back to Search Results
Model Number CI-1601-05
Device Problems Adverse Event Without Identified Device or Use Problem (2993); No Apparent Adverse Event (3189)
Patient Problem Hemorrhage/Bleeding (1888)
Event Date 03/02/2021
Event Type  Injury  
Event Description
The recipient reportedly experienced post procedure complications with hemorrhaging.The recipient was hospitalized for the night.The recipient is doing well.Advanced bionics is in the process of obtaining additional information.When additional information is received, a supplemental report will be submitted.
 
Manufacturer Narrative
Advanced bionics no longer considers this event reportable.The recipient reportedly did not receive medical intervention.This is the final report.Disclaimer: advanced bionics does not intend that this report be any admission of liability, fault or product defect.
 
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Brand Name
HIRES ULTRA 3D IMPLANT
Type of Device
COCHLEAR IMPLANT
Manufacturer (Section D)
ADVANCED BIONICS, LLC
28515 westinghouse place
valencia CA 91355
MDR Report Key11624886
MDR Text Key244153219
Report Number3006556115-2021-00326
Device Sequence Number1
Product Code MCM
UDI-Device Identifier07630016878008
UDI-Public(01)07630016878008(11)210106(17)231231
Combination Product (y/n)N
PMA/PMN Number
P960058
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type user facility
Type of Report Initial,Followup
Report Date 03/08/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/06/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Expiration Date12/31/2023
Device Model NumberCI-1601-05
Was Device Available for Evaluation? No
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Hospitalization; Required Intervention;
Patient Age87 YR
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