Model Number 3186 |
Device Problem
Unintended Movement (3026)
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Patient Problems
Fall (1848); Inadequate Pain Relief (2388)
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Event Date 12/06/2014 |
Event Type
Injury
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Event Description
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Device 2 of 2.Reference mfr report: 1627487-2014-02883.
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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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Device 2 of 2
reference mfr report: 1627487-2014-02883.
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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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Device 2 of 2.Reference mfr report: 1627487-2014-02883.
|
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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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Device 2 of 2.Reference mfr report: 1627487-2014-02883.
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Manufacturer Narrative
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Manufacturer evaluation: the returned product was not analyzed as the complaint of lead migration could not be confirmed via laboratory testing.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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