MAUDE Adverse Event Report: OTICON MEDICAL - NEURELEC NEURO ZTI COCHLEAR IMPLANT; NEURO ZTI EVO

Model Number	NEURO ZTI EVO
Medical Device Problem Code	Connection Problem (2900)
Health Effect - Clinical Codes	Failure of Implant (1924); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/21/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The oticon medical representative reported that no connection to the neuro zti evo implant could be established despite different configurations tested: antenna changes, use of magnets of different strengths and other processors (neuro 2 and neuro one).The oticon medical representative also reported that the patient did not experience any mishaps or hits on his head.No in vivo assessment report was received.Udi: (b)(4).
Event or Problem Description
The oticon medical representative reported that no connection to the neuro zti evo implant could be established despite different configurations tested : antenna changes, use of magnets of different strengths and other processors (neuro 2 and neuro one).The oticon medical representative also reported that the patient did not experience any mishaps or hits on his head.
Additional Manufacturer Narrative
The oticon medical representative reported that no connection to the neuro zti evo implant could be established despite different configurations tested : antenna changes, use of magnets of different strengths and other processors (neuro 2 and neuro one).The oticon medical representative also reported that the patient did not experience any mishaps or hits on his head.No in vivo assessment report was received.Udi : (b)(4).While this device has gained initial pma approval, it has not been commercialized, imported or sold in the us and no implantations have been performed as of the date of this report.The subject device is part of the voluntary field corrective action initiated for neuro zti on october 14th, 2021 (international recall #211014).
Event or Problem Description
The oticon medical representative reported that no connection to the neuro zti evo implant could be established despite different configurations tested : antenna changes, use of magnets of different strengths and other processors (neuro 2 and neuro one).The oticon medical representative also reported that the patient did not experience any mishaps or hits on his head.

• Brand Name: NEURO ZTI COCHLEAR IMPLANT
• Common Device Name: NEURO ZTI EVO
• Manufacturer (Section D): OTICON MEDICAL - NEURELEC; 2720, chemin saint-bernard; porte 14; vallauris, 06220 ; FR 06220
• Manufacturer Contact: adrian ternisien ; 2720, chemin saint-bernard; porte 14; vallauris, 06220 ; FR 06220
• MDR Report Key: 14875561
• Report Number: 3016743107-2022-00003
• Device Sequence Number: 20265743
• Product Code: MCM
• UDI-Device Identifier: 03663227801859
• UDI-Public: (01)03663227801859(11)201103(17)231103
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: P200021
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 08/28/2022

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?: Yes
• Operator of Device: Lay User/Patient
• Device Expiration Date: 11/03/2023
• Device Model Number: NEURO ZTI EVO
• Device Catalogue Number: M80185
• Device Lot Number: 20-04818
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/21/2022
• Supplement Date Received by Manufacturer: 02/21/2022
• Initial Report FDA Received Date: 06/30/2022
• Supplement Report FDA Received Date: 08/28/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/03/2020
• 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: Unknown