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Recall Observatory FDA recall evidence

Device product

OSCOR ADELANTE BREEZEWAY 10F C70¿ S61CM D66CM Catalog # AB101073 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.

Z-0801-2017

October 05, 2016

Class II

Product summary

Firm
Oscor, Inc.
Event
Event 75785
Status
Terminated
Classification
Class II
Quantity
70
Official record key
device-enforcement:Z-0801-2017

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: C1-09395 Exp. November 17, 2017 and C1-11621 Exp. November 2, 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.