Model Number 382400 |
Device Problem
Output below Specifications (3004)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/22/2017 |
Event Type
malfunction
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Manufacturer Narrative
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Submit date: 03/08/2017.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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Event Description
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The customer reports: low feed.
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Manufacturer Narrative
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This report was filed in error as it is a duplicate of a report already filed under 2183870-2017-00118.
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Event Description
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The customer reports: low feed.
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Manufacturer Narrative
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The previous supplemental report stating that this report was submitted in error was false.This report was originally submitted correctly.Please see the investigation results below.As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.The unit was sent to a service center for repair.Upon triage, a technician found that the volume being delivered during testing was within specifications.The unit has been recertified per procedure.
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Event Description
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The customer reports: low feed.
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Search Alerts/Recalls
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