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

Model Number	93550
Medical Device Problem Codes	Signal Artifact/Noise (1036); Inadequacy of Device Shape and/or Size (1583)
Health Effect - Clinical Codes	Pain (1994); Discomfort (2330)
Date of Event	01/13/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
Per the clinic, the patient experienced pain at the magnet site.The patient wore a soft pad to achieve adequate retention; however, the patient continued to experience discomfort and pain due to the tightness and strength of the magnet connection to the implant.A reduced-strength magnet did not provide adequate retention.Due to the pain, the patient was unable to wear the processor for extended periods of time.The patient also reported discomfort with sound quality in noisy environments and excessive acoustic feedback from the processor.Subsequently, the internal magnet was explanted under general anesthesia on (b)(6) 2026 and the patient was reimplanted with another cochlear device during the same surgery.

• Brand Name: BIM400 IMPLANT MAGNET
• Common Device Name: COCHLEAR BAHA ATTRACT SYSTEM
• Manufacturer (Section D): COCHLEAR BONE ANCHORED SOLUTIONS AB; konstruktionsvägen 14; mölnlycke, 435 3 3; SW 435 33
• MDR Report Key: 24442060
• Report Number: 6000034-2026-00672
• Device Sequence Number: 10364000
• Product Code: LXB
• UDI-Device Identifier: 09321502025294
• UDI-Public: (01)09321502025294(10)110452(17)210211
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 02/25/2026
• Report Date (Section F): 02/25/2026

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
• Operator of Device: Lay User/Patient
• Device Expiration Date: 02/11/2021
• Device Model Number: 93550
• Device Catalogue Number: 93550
• Device Lot Number: 110452
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/18/2026
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 01/31/2026
• Date Report to Manufacturer: 01/31/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 02/25/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 54 YR
• Patient Sex: Unknown
• Date Report Sent to FDA: 02/25/2026