Model Number KNEE SCORPION |
Device Problem
Defective Device (2588)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/02/2024 |
Event Type
malfunction
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Manufacturer Narrative
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The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.The root cause of the event could not be determined from the information available and without device evaluation.
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Event Description
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On 02/02/2024, it was reported by a sales representative via (b)(4) that an ar-12990 knee scorpion had 3 needles break while using the device.Everything was retrieved.No patient was harmed.
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Search Alerts/Recalls
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