Z-0799-2017 Class II Terminated
FDA device recall Z-0799-2017 was initiated by Oscor, Inc. on October 5, 2016 and is designated Class II. Reason for recall: Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use. The recall status is terminated (terminated July 26, 2019). Affected quantity: 21.
Recall Details
- Product Type
- Devices
- Report Date
- December 28, 2016
- Initiation Date
- October 5, 2016
- Termination Date
- July 26, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 21
Product Description
OSCOR ADELANTE BREEZWAY 8F STRAIGHT S79CM D84CM Catalog # AB081211 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.
Reason for Recall
Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
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
Code Information
Lot #'s: C1-08988 Exp. June 1, 2017, C1-08988 Exp. June 1, 2017, OR-04708 Exp. August 19, 2018, C1-08988 Exp. June 1, 2017, C1-08988 Exp. June 1, 2017, C1-09373 Exp. November 5, 2017, C1-09373 Exp. November 5, 2017, OR-04708 Exp. August 19, 2018, and C1-11734 Exp. October 5, 2018