U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
arterial cannula - Product Code DSQ
원인
During use an unexpected flaking of the inner surface coating (blood contact) that has the potential for risk of embolism.
조치
On 1/26/2004, the firm issued letters via Federal Express to all its direct consignees, informing them of the affected product and providing instructions on the recall.
Nationwide to 11(eleven) hospitals. The product was shipped within the United States in IL, MA, NC, MD, MO, FL, CA, AZ, PA, and NY. The product was distributed to one consignee in Australia.
제품 설명
Thoratec brand Sealed Arterial Cannula for use with the Thoratec Vascular Assist Device System, || Model Number(s): Catalogue numbers: || #100118-- Short, 14mm graft; || #100121-- Long, 14mm graft; || #100129-- Long, 18mm graft. || Manufactured by Thoratec Corporation, 6035 Stoneridge Drive, Pleasanton, CA 94588