TITAN SPINE, LLC ENDOSKELETON TAS 7 DEG LORDOCTIC, IMPLANT STANDARD, 10MM; INTERBODY FUSION DEVICE
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Catalog Number 2307-0110 |
Device Problem
Bent (1059)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 01/24/2018 |
Event Type
malfunction
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Manufacturer Narrative
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The device was not fully inserted and was removed from the surgical site as a result of the malfunction.The surgical procedure was completed using a 12 deg titan spine implant, which has a smaller posterior ht.The sales rep reported that they were no issues while inserting this device.The patient was not harmed as a result of the malfunction.
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Event Description
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During a alif procedure, a quantity of 2 endoskeleton tas ibd's broke and/or bent during insertion upon impaction.
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Search Alerts/Recalls
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