Model Number TPS111111101 |
Device Problems
Device Operates Differently Than Expected (2913); Noise, Audible (3273)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 04/01/2018 |
Event Type
Injury
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Manufacturer Narrative
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It was reported that the procedure for the debridement of soft tissue was performed for a patient with an itotal knee replacement due to a patella crepitation.Review of the device history record indicates that the device was manufactured to specification.
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Event Description
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It was reported that the procedure for the debridement of soft tissue was performed for a patient with an itotal knee replacement due to a patella crepitation.
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Search Alerts/Recalls
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