Model Number 3183ANS |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Muscle Spasm(s) (1966)
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Event Type
Injury
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Event Description
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Device 2 of 2.Reference mfr report #: 1627487-2015-07040.
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Event Description
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Device 2 of 2 reference mfr report #: 1627487-2015-07040.
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Manufacturer Narrative
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Udi (di): (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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Manufacturer Narrative
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Evaluation codes (continued): results code: the complaint could not be confirmed for muscle spasms.Visual inspection and functional testing did not show any anomalies.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 #: 1627487-2015-07040.
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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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