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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: COCHLEAR BONE ANCHORED SOLUTIONS AB BIM400 IMPLANT MAGNET; COCHLEAR BAHA ATTRACT SYSTEM

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COCHLEAR BONE ANCHORED SOLUTIONS AB BIM400 IMPLANT MAGNET; COCHLEAR BAHA ATTRACT SYSTEM Back to Search Results
Model Number 93550
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Post Operative Wound Infection (2446); Fluid Discharge (2686)
Event Type  Injury  
Manufacturer Narrative
This report is submitted on december 18, 2020.
 
Event Description
Per the clinic, the patient experienced an infection and discharge at the incision site, and was treated with steroids and antibiotics (duration and date not reported).The implanted device remains.Explantation is planned but has not taken place at the time of this report.
 
Manufacturer Narrative
It was reported that the internal magnet was explanted on (b)(6) 2020.This report is submitted on 10 february 2021.
 
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Brand Name
BIM400 IMPLANT MAGNET
Type of Device
COCHLEAR BAHA ATTRACT SYSTEM
Manufacturer (Section D)
COCHLEAR BONE ANCHORED SOLUTIONS AB
konstruktionsvägen 14
po box 82
mölnlycke, 435 2 2
SW  435 22
MDR Report Key11032708
MDR Text Key222283088
Report Number6000034-2020-03655
Device Sequence Number1
Product Code LXB
Combination Product (y/n)N
PMA/PMN Number
K131240
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type health professional
Type of Report Initial,Followup
Report Date 01/18/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model Number93550
Device Catalogue Number93550
Device Lot Number130947
Was Device Available for Evaluation? No
Initial Date Manufacturer Received 11/30/2020
Initial Date FDA Received12/17/2020
Supplement Dates Manufacturer Received01/18/2021
Supplement Dates FDA Received02/09/2021
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
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