MAUDE Adverse Event Report: Cochlear Bone Anchored Solutions AB BIA300 Implant 4mm w Abutment 6mm; Cochlear Baha Connect System

Model Number	92127
Medical Device Problem Codes	Loss of Osseointegration (2408); Expulsion (2933)
Health Effect - Clinical Codes	Inadequate Osseointegration (2646); Skin Infection (4544)
Type of Reportable Event	Serious Injury
Event or Problem Description
Per the clinic, the patient experienced partial implant extrusion following head trauma from a pillow, with subsequent infection and loss of osseointegration resulting in fixture loss.The patient was reimplanted with another device on (b)(6), 2026.Additional information has been requested but has not been made available as of the date of this report.

• Brand Name: BIA300 Implant 4mm w Abutment 6mm
• Common Device Name: Cochlear Baha Connect System
• Manufacturer (Section D): Cochlear Bone Anchored Solutions AB; konstruktionsvägen 14; mölnlycke, 435 3 3; SW 435 33
• Manufacturer (Section G): Cochlear Bone Anchored Solutions AB; konstruktionsvägen 14; mölnlycke, 435 3 3; SW 435 33
• Manufacturer Contact: amalia azman ; unit ug-1 vertical podium; no. 8 jalan kerinchi; kuala lumpur, wilayah persekutuan 59200 ; MY 59200
• MDR Report Key: 50774540
• Report Number: 6000034-2026-03237
• Device Sequence Number: 21200326
• Product Code: LXB
• UDI-Device Identifier: 09321502019521
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: K100360
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Type of Report: Initial
• Report Date (Section B): 09/15/2026

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: 06/30/2017
• Device Model Number: 92127
• Device Catalogue Number: 92127
• Device Lot Number: 125092
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 08/19/2026
• Initial Report FDA Received Date: 09/15/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Female