Catalog Number 7222120000 |
Device Problems
Fracture (1260); Difficult to Open or Close (2921)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 12/25/2018 |
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: 1 event was reported for this quarter.Product return status: 1 device investigation type has not yet been determined.Evaluation status: 1 device evaluation is in progress.Additional information: 1 device is not labeled for single-use.1 device was not reprocessed and reused.
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Event Description
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This report summarizes 1 malfunction event in which the device fractured and had difficulty opening and closing.1 event had patient involvement; no patient impact.
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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: 1 previously reported event is included in this follow-up record. product return status 1 device was not available for evaluation.
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Event Description
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This report summarizes 1 malfunction event in which the device fractured and had difficulty opening and closing.1 event had patient involvement; no patient impact.
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Search Alerts/Recalls
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