Model Number 8120 |
Device Problems
Device Alarm System (1012); Calibration Problem (2890); Naturally Worn (2988)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 07/26/2023 |
Event Type
malfunction
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Manufacturer Narrative
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A device history record review is performed on each device reported in a mdr reportable event along with other methods of investigation as coded in section h6 of this mdr report.Per 803.52(f)(11)(iii) the information provided was obtained from servicing activities performed on the device.There were no additional details obtainable or provided at the time of service.H3 other text : see manufacturer narrative.
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Event Description
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It was reported that the device had failed binary switches.There was no patient involvement.
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Event Description
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It was reported that the device had failed binary switches.There was no patient involvement.
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Manufacturer Narrative
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Correction: annex b: b21 annex c: c21 annex d: d16 additional information: device available for eval?, returned to manufacturer on, device return to manuf.?, device eval by manufacturer?, annex a: a040507 annex b: b01 annex c: c070606 annex d: d02 annex g: g04061.
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Event Description
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It was reported that the device had failed binary switches.There was no patient involvement.
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Search Alerts/Recalls
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