Catalog Number 5407120470 |
Device Problem
Detachment of Device or Device Component (2907)
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Patient Problems
Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/31/2023 |
Event Type
malfunction
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Manufacturer Narrative
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This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events: 2 events were reported for this quarter.Product return status: 2 device investigation types have not yet been determined.Additional information: 2 devices were not labeled for single-use.2 devices were not reprocessed or reused.
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Event Description
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This report summarizes 2 malfunction events in which the device had a component detach.- 1 event had no patient involvement; no patient impact.- 1 event had insufficient information received.
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Manufacturer Narrative
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This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Supplemental rationale corrected data: b5, h6, h11 2 previously reported events are included in this follow-up record.Product return status 1 device was received.1 device was not available for evaluation.
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Event Description
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This report summarizes 2 malfunction events in which the device had a component detach.- 1 event had no patient involvement; no patient impact.- 1 event had patient involvement; no patient impact.
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Search Alerts/Recalls
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