Catalog Number 352506070E |
Device Problems
Migration or Expulsion of Device (1395); Failure to Align (2522)
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Patient Problem
Perforation (2001)
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Event Date 09/13/2017 |
Event Type
Injury
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Manufacturer Narrative
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The device has not been returned for evaluation and no images or videos have been provided of the filter in-vivo, so the complaint cannot be confirmed.If additional information is provided in the future, this issue will be re-evaluated as needed.
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Event Description
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According to the notice received by way of a civil action complaint filed on (b)(6) 2020, the patient was prescribed and implanted with an option elite retrievable ivc filter on or about (b)(6) 2017 by (b)(6).The patient scheduled a retrieval procedure on or about (b)(6) 2019 by (b)(6); the filter was able to be retrieved.The complaint alleges tilt and perforation.Argon¿s attorneys are attempting to gather additional information.
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Search Alerts/Recalls
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