Catalog Number UNKNOWN |
Device Problems
Entrapment of Device (1212); Migration (4003)
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Patient Problem
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
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Event Date 03/30/2011 |
Event Type
Injury
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Manufacturer Narrative
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The device is indicated as unavailable for evaluation.Without the device or any images in-vivo to review, the complaint cannot be confirmed.If additional information is received in the future, a follow-up report will be provided.
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Event Description
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According to the notice received by way of a civil action complaint, the patient was prescribed and implanted with an option vena cava filter on or about (b)(6) 2011 by dr.(b)(6).The complaint alleges there was embedment and tilt post-implant.The filter was not able to be retrieved.Argon¿s attorneys are attempting to gather additional information.
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Search Alerts/Recalls
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