Model Number 26816 |
Device Problem
Low Readings (2460)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 01/01/1901 |
Event Type
malfunction
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Manufacturer Narrative
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The product has been returned to the local facility but has not yet been received at the main office for evaluation.Once returned and investigated, a follow-up report will be submitted.
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Event Description
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The customer reported that the device provided low readings.No consequences or impact to patient were reported.
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Manufacturer Narrative
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Additional manufacuring narrative: the returned device was evaluated.During evaluation the device passed all visual and functional testing.During simulation testing, the device passed manual and preset conditions and provided accurate measurements.The unit was found to visually and audibly alarm during alarm conditions.The unit was determined to be functioning as designed.
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Event Description
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The customer reported that the device provided low readings.No consequences or impact to patient were reported.
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Search Alerts/Recalls
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