Model Number 102096-67A |
Device Problem
Failure to Sense (1559)
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Patient Problems
No Known Impact Or Consequence To Patient (2692); No Information (3190)
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Event Date 11/14/2019 |
Event Type
malfunction
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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) 2019, the sensor experienced an early sensor retirement thereby requiring early removal of the inserted device.
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Manufacturer Narrative
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The return material authorization (rma) was authorized but not received so no further confirmation or investigation of the complaint is possible.
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Search Alerts/Recalls
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