Model Number 102096-67A |
Device Problem
Difficult to Remove (1528)
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Patient Problem
Discomfort (2330)
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Event Date 10/13/2020 |
Event Type
Injury
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Manufacturer Narrative
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The manufacturer is currently performing an investigation and will provide the results with the supplemental report.
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Event Description
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On (b)(6) 2020, senseonics was made aware of an adverse event where the physician was unable to remove the sensor on the first attempt made.
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Manufacturer Narrative
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Per case notes.Sensor was successfully removed.D2: product code changed to qhj; h6: investigation findings, changed to 3221; h6: investigation conclusions, changed to 4311.
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Search Alerts/Recalls
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