Model Number 1515 |
Device Problem
Suction Problem (2170)
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Patient Problem
Insufficient Information (4580)
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Event Date 04/21/2021 |
Event Type
malfunction
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Manufacturer Narrative
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Investigation, including root cause analysis, is in progress.A supplemental mdr will be filed as necessary in accordance with 21 cfr 803.56 when additional reportable information becomes available.The manufacturer internal reference number is: (b)(4).
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Event Description
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A customer reported loss of suction with a patient interface (pi).Additional information has been requested.There are multiple related reports for this facility.This report addresses (b)(4) and other manufacturer reports will be filed.
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Manufacturer Narrative
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A review of the device history record traceable to the reported lot number indicates that the product was processed and released according to the product¿s acceptance criteria.The root cause could not be determined conclusively.The manufacturer internal reference number is: (b)(4).
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Search Alerts/Recalls
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