Catalog Number 3300000020 |
Device Problems
Break (1069); Device Slipped (1584)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 02/13/2014 |
Event Type
malfunction
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Event Description
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It was reported via repair work order that the mechanism was broken and would not latch.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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Follow-up submitted with evaluation results.Recliner was replaced.
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Event Description
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It was reported via repair work order that the mechanism was broken and would not latch.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
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Search Alerts/Recalls
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