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Model Number SCORPION NEEDLE, KNEE |
Device Problem
Break (1069)
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Patient Problem
Foreign Body In Patient (2687)
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Event Date 03/15/2024 |
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.If the device becomes available for evaluation, a follow-up report will be submitted.
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Event Description
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On 3/18/2024, it was reported by an arthrex subsidiary employee via (b)(4) that an ar-12990n scorpion needle broke."since the part was difficult to retrieve, it could not be retrieved and remained in the patient.The surgery was completed by using a new product with same part number." additional information requested.
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Search Alerts/Recalls
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