Catalog Number 41894 |
Device Problem
No Flow (2991)
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Patient Problem
No Patient Involvement (2645)
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Event Date 07/07/2016 |
Event Type
malfunction
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Manufacturer Narrative
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Qn#(b)(4).The device sample was returned to the manufacturer, but the results of the investigation are pending at the time of this report.
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Event Description
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The customer alleges that the nebulizer did not produce mist when pre-tested for patient use.
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Manufacturer Narrative
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Qn#(b)(4).The sample was returned for evaluation.A visual exam was performed and no defects were observed.Functional testing was also performed and no issues were found.The sample was within specification.Based on the investigation performed, the reported complaint could not be confirmed.There were no issues found with the returned sample.
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Event Description
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The customer alleges that the nebulizer did not produce mist when pre-tested for patient use.
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Search Alerts/Recalls
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