Model Number 3789 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Increased Sensitivity (2065); Swelling (2091); Post Operative Wound Infection (2446)
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Event Date 12/21/2014 |
Event Type
Injury
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Event Description
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It was reported the patient experienced fever along with swelling and redness at the ipg site.The physician prescribed antibiotics to the patient.
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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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Event Description
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Further follow up identified the patient met with sjm representative for reprogramming and the patient is doing "good".
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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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Search Alerts/Recalls
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