FDA Enforcement
Class II
Terminated
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.
Recall: Z-0818-2017
·
Reported December 28, 2016
Enforcement
- Recall Number
- Z-0818-2017
- Event ID
- 75785
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Oscor, Inc.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Report Date
- December 28, 2016
- Initiation Date
- October 5, 2016
- Classification Date
- December 19, 2016
- Termination Date
- July 26, 2019
- Address
- 3816 Desoto Blvd, N/A, Palm Harbor, FL, 34683-1618, United States
Description
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.
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 Info
Lot #'s: C1-12493 Exp. May 5, 2019
Distribution
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
Quantity
55