Model Number 3183 |
Device Problems
Kinked (1339); Impedance Problem (2950)
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Patient Problem
Inadequate Pain Relief (2388)
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Event Type
Injury
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Manufacturer Narrative
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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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Manufacturer Narrative
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Results: complaint was confirmed for loss of stimulation.As received, the microscopic inspection of the lead body segment revealed a lead breakage with all wires broken and a compression mark.The compression mark and breakage on the lead when align correspond to distal end of a swift lock anchor.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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It was reported the patient ((b)(6)) lost stimulation.Lead diagnostic testing revealed invalid impedance measurements.X-rays identified a kink in the lead near the anchor site.In turn, the patient underwent surgical intervention to explant and replace the lead and anchor which resolved the issue.The date the patient lost stimulation is unknown.Concomitant products: the implant date for the following device is unknown: model: 3788, scs ipg, model: 3383, scs extension.
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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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Search Alerts/Recalls
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