Catalog Number UNK_SPE |
Device Problems
Adverse Event Without Identified Device or Use Problem (2993); No Apparent Adverse Event (3189)
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Patient Problems
Dysphagia/ Odynophagia (1815); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/01/2018 |
Event Type
Injury
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Manufacturer Narrative
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Return status is unknown.
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Event Description
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Through a clinical study, it was reported that six (6) patients experienced dysphagia post-operatively.Implant dates provided as 'january 2018 to august 2020'.Explant dates have not been provided.Device information provided as 'capri® cervical 3d expandable corpectomy cage system'.No further details have been reported.This report will capture the fourth of six patients.
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Manufacturer Narrative
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Additional information provided by the operating physician indicates the device did not cause or contribute to the reported events.The events were a result of pre-existing patient conditions.
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Event Description
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Through a clinical study, it was reported that six (6) patients experienced dysphagia post-operatively.Implant dates provided as (b)(6) 2018 to (b)(6) 2020'.Explant dates have not been provided.Device information provided as 'capri® cervical 3d expandable corpectomy cage system'.No further details have been reported.This report will capture the fourth of six patients.
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Search Alerts/Recalls
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