Concomitant medial product: arctic front advance cardiac cryoablation catheter.Medtronic was made aware of this event through a search of literature publications.It was not possible to ascertain specific patient or device information from the literature publication or to match the event with previously reported events.This information is based entirely on journal literature.This event occurred outside the us.All information provided is included in this report.Patient information is limited due to confidentiality concerns.The baseline gender/age of the patients represented in the article is male/63 years old.The model listed in the report is a representative, as there is no specific model listed.Multiple patients were noted in the article; however, a one to one correlation could not be made with unique product lot numbers.Without a lot number or device serial number, the manufacturing date cannot be determined.Since no device id was provided, it is unknown if this event has been previously reported.Referenced article: ¿how safe are noacs compared with phenprocoumon after pulmonary vein isolation with the cryoballoon technique using purse-string suture closure?¿ int j cardiol (2017), http://dx.Doi.Org/10.1016/j.Ijcard.2017.06.077.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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The literature publication reports the following patient complication while using a sheath catheter: multiple patients were noted in the article; however, a one to one correlation could not be made with unique product lot numbers.There were two (2) patients with pericardial effusion, neither of which required pericardiocentesis.The status/location of the sheath catheter is unknown.No further patient complications have been reported as a result of this event.
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