Catalog Number SRD06005045L |
Device Problem
Patient Device Interaction Problem (4001)
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Patient Problem
Unspecified Infection (1930)
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Event Date 09/08/2019 |
Event Type
Injury
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Manufacturer Narrative
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The review of the manufacturing paperwork verified that the lot met all pre-release specifications.As the device was not returned, no evaluation of the device could be performed.
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Event Description
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On (b)(6) 2019, the patient underwent a right femoral artery loop procedure with a gore-tex® stretch vascular graft - standard-walled fixed ringed.The device was reportedly used for the application of av access.It is unknown if the device was pre-cannulated for av access.There was reportedly no pre-existing infection at implant site.On (b)(6) 2019, the device was reportedly explanted due to infection.The physician reportedly stated it is unknown if the cause of the infection is attributed to the gore device.
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Manufacturer Narrative
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H6: code 213 ¿ the review of the sterilization paperwork verified that the lot met all pre-release specifications.
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Search Alerts/Recalls
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