Catalog Number 0250070620 |
Device Problem
Device Contamination with Chemical or Other Material (2944)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 06/11/2015 |
Event Type
malfunction
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Event Description
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It was reported that white residue was found on the probe of the product.The white residue was noticed at the beginning of the case when they were opening the packaging.
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Manufacturer Narrative
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Additional information will be provided once the investigation has been completed.
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Manufacturer Narrative
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The particle/debris condition was not confirmed since the unit was not received.As per risk document likely root causes are: manufacturing/assembly error.Incorrect or inadequate packaging.Severe shipping conditions.The product was not returned for investigation therefore the reported failure mode was not confirmed.The failure mode will be monitored for future reoccurrence.
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Event Description
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It was reported that white residue was found on the probe of the product.The white residue was noticed at the beginning of the case when they were opening the packaging.
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Search Alerts/Recalls
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