Model Number SC-1110-02 |
Device Problems
Device Inoperable (1663); Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
No Known Impact Or Consequence To Patient (2692); No Information (3190)
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Event Date 04/22/2018 |
Event Type
Injury
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Manufacturer Narrative
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The explanted device was not returned to bsn as it was kept by medical facility.
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Event Description
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A report was received that the patient underwent an ipg replacement procedure for an unknown reason.No device malfunction was suspected.The patient was doing well postoperatively.
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Manufacturer Narrative
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Additional information was received that the reason for ipg replacement was due to non-functional battery.It was also reported that there was no issue with the device and it was time to have a new battery.
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Event Description
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A report was received that the patient underwent an ipg replacement procedure for an unknown reason.No device malfunction was suspected.The patient was doing well postoperatively.
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Search Alerts/Recalls
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