Model Number MI1200 SYNCHRONY PIN |
Device Problems
Adverse Event Without Identified Device or Use Problem (2993); Insufficient Information (3190)
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Patient Problems
Unspecified Infection (1930); Post Operative Wound Infection (2446); Skin Tears (2516)
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Event Type
Injury
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Manufacturer Narrative
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The device has not been explanted.If it should be explanted, it is to be returned to the manufacturer for evaluation.When available, a device failure analysis will be submitted as a follow up report.
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Event Description
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Recipient reported swelling at the implant site since the device was implanted on (b)(6) 2019.He was examined by physician about oozing of pus from the incision area on (b)(6) 2019.It was suspected that there was an infection.According to information received on the november 21, 2019, the infection was under control.It is believed that the user experienced a contact dermatitis from the external equipment that spread internally.The user has started using his device again.As of information received on the 9th march 2020 the infection did flare up again and therefore the user will be explanted.
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Event Description
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Recipient reported swelling at the implant site since implantation.The user was examined about oozing of pus from the incision area on (b)(6) 2019 and it was suspected that there was an infection.On (b)(6) 2019, culture results showed growth of staphylococcus aureus.Also, the user has always had a hard time with retention.There was some speech understanding but due to retention issues the user had not adjusted to his device.It is believed that the user experienced a contact dermatitis from the external equipment that spread internally.As of information received in march 2020 the infection did flare up again and therefore the user will be explanted.The explantation had to be cancelled with no new planned date.
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Manufacturer Narrative
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Additional information: according to the information received from the field the recipient suffered from an infection at the incision three months after implantation.A review of the device's sterilization records shows that the device has been subject to a valid sterilization process.Reportedly, the recipient suffered from a contact dermatitis, which might has contributed to the infection.Furthermore, information on the implant registration card states that two channels were left outside of cochlea at initial implantation.In addition, the recipient experienced retention issues with the device, which were most likely caused by the reported swelling over the implant site.Revision surgery had to be cancelled and no date has been scheduled yet.
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Event Description
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Recipient reported swelling at the implant site since the device was implanted on (b)(6)2019.The user was examined by physician about oozing of pus from the incision area on (b)(6)2019.According to information received on the (b)(6)2019, the infection was under control.It is believed that the user experienced a contact dermatitis from the external equipment that spread internally.The user started using his device again.However, the infection flared up again and therefore the user was explanted on the (b)(6)2020.
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Manufacturer Narrative
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Additional information: according to the information received from the field the recipient suffered from a re-occuring infection at the incision since three months after implantation.A review of the device_s sterilization records shows that the device has been subject to a valid sterilization process.Reportedly, the recipient suffered from a contact dermatitis, which might have contributed to the infection.Furthermore, information on the implant registration card states that two channels were left outside of cochlea at initial implantation.In addition, the recipient experienced retention issues with the device, which were most likely caused by the reported swelling over the implant site.The concerned device was explanted but is not available for investigation.
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Search Alerts/Recalls
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