Catalog Number 4701000000 |
Device Problems
Break (1069); Scratched Material (3020)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 11/07/2014 |
Event Type
malfunction
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Event Description
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It was reported via repair work order that the foot section weldment was damaged with exposed sharp edges reported.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 foot section weldment was damaged with exposed sharp edges reported.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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Supplemental report submitted to include 510(k)# for the product.
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Search Alerts/Recalls
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