Catalog Number 2950100002 |
Device Problems
Contamination (1120); Material Discolored (1170)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 12/27/2013 |
Event Type
malfunction
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Event Description
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It was reported via repair work order that the mattress was discolored due to fluid intrusion.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Event Description
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It was reported via repair work order that the mattress was discolored due to fluid intrusion.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Manufacturer Narrative
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Replaced mattress.
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Manufacturer Narrative
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Follow-up submitted as this complaint was previously reported in medwatch #0001831750-2013-09003.
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Search Alerts/Recalls
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