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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COCHLEAR BONE ANCHORED SOLUTIONS AB FLANGE FIXTURE AND ABUTMENT LXB

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COCHLEAR BONE ANCHORED SOLUTIONS AB FLANGE FIXTURE AND ABUTMENT LXB Back to Search Results
Model Number BIM400
Device Problem Insufficient Information (3190)
Patient Problems Hematoma (1884); Swelling (2091)
Event Date 07/05/2016
Event Type  Injury  
Manufacturer Narrative

(b)(4). This report is filed on (b)(6) 2016. Implanted device remains.

 
Event Description

Per the clinic, the patient experienced swelling and hematoma at implant site, however the issue did not resolve. Subsequently, the patient underwent revision surgery on (b)(6) 2016 to drain the hematoma. The implanted device remains.

 
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Brand NameFLANGE FIXTURE AND ABUTMENT
Type of DeviceLXB
Manufacturer (Section D)
COCHLEAR BONE ANCHORED SOLUTIONS AB
konstruktionsvägen 14
po box 82
mölnlycke, 435 2 2
SW 435 22
Manufacturer Contact
kristel kohne
1 university avenue
macqaurie university, nsw 2109
AS   2109
2 9428 655
MDR Report Key5784540
MDR Text Key49231904
Report Number6000034-2016-01429
Device Sequence Number1
Product Code LXB
Combination Product (Y/N)N
Reporter Country CodeNZ
PMA/PMN NumberK131240
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type HEALTH PROFESSIONAL
Reporter Occupation HEALTH PROFESSIONAL
Type of Report Initial
Report Date 07/07/2016
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received07/12/2016
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator LAY USER/PATIENT
Device MODEL NumberBIM400
Device Catalogue Number93550
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received07/07/2016
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

Patient TREATMENT DATA
Date Received: 07/12/2016 Patient Sequence Number: 1
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