Model Number 3286 |
Device Problem
Torn Material (3024)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/15/2016 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).Sjm has limited information related to the patient's medical history and is unable to form an opinion as to the relevancy of the patient's history to the event reported.Sjm defers to the patient's physician regarding medical history.
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Event Description
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Device #1 of 2: reference mfr.Report:1627487-2016-01138: it was reported during the procedure to remove and replace the ipg (normal end of life) the leads were cut, hence the leads were removed and replaced.The patient is receiving effective stimulation.
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Manufacturer Narrative
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(b)(4).
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Event Description
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Device #1 of 2: reference mfr.Report:1627487-2016-01138.
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Manufacturer Narrative
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(b)(4).
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Event Description
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Device #1 of 2: reference mfr.Report:1627487-2016-01138.
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Event Description
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Device #1 of 2: reference mfr.Report:1627487-2016-01138.
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Search Alerts/Recalls
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