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Catalog Number C01A |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problem
Pain (1994)
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Event Type
Injury
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Manufacturer Narrative
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Neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation.Therefore, we are unable to determine the definitive cause of the reported event.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
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Event Description
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It was reported that on an unknown date, patient was presented with primary diagnosis osteoporosis and patient had compression fracture at level l2.Post-op, there was remaining nrs score (pain score).The patient haven't underwent the back pain check-up since a month for follow up visit.
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Search Alerts/Recalls
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