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Recall Observatory FDA recall evidence

Device product

MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL Catalog # 990061-090-000 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.

Z-0813-2017

October 05, 2016

Class II

Product summary

Firm
Oscor, Inc.
Event
Event 75785
Status
Terminated
Classification
Class II
Quantity
215
Official record key
device-enforcement:Z-0813-2017

Official wording

Reason: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.

Code information: Lot #'s: C1-08939 Exp. May 19, 2017, C1-08985 Exp. June 1, 2017, C1-09584 Exp. January 18, 2018, and C1-10120 Exp. April 17, 2018

Distribution pattern: Worldwide Distribution - US including CA, NJ, MD, TX, FL, NC, MO, and Puerto Rico. Internationally to AUSTRIA, BOLIVIA, CANADA, CHILE, CYPRUS, NETHERLANS, EGYPT, GERMANY, HONG KONG, ISRAEL, ITALY, SWITZERLAND, and VIETNAM

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.