P-014 Reperfusion catheter malfunction during stroke intervention: an analytical review of the FDA’s...
P-014 Reperfusion catheter malfunction during stroke intervention: an analytical review of the FDA’s maude database
About this item
Full title
Author / Creator
Bageac, D , Gershon, B and De Leacy, R
Publisher
London: BMJ Publishing Group LTD
Journal title
Language
English
Formats
Publication information
Publisher
London: BMJ Publishing Group LTD
Subjects
More information
Scope and Contents
Contents
BackgroundIn December 2020, the JET7 Xtra Flex reperfusion catheter was voluntarily recalled after reports of injury and death associated with device malfunction. The FDA’s MAUDE (Manufacturer and User Facility Device Experience) database aggregates reports of adverse events and product problems involving medical devices. We present the first analy...
Alternative Titles
Full title
P-014 Reperfusion catheter malfunction during stroke intervention: an analytical review of the FDA’s maude database
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_journals_2555266530
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2555266530
Other Identifiers
ISSN
1759-8478
E-ISSN
1759-8486
DOI
10.1136/neurintsurg-2021-SNIS.50
