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
Needle, aspiration and injection, reusable - Product Code GDM
원인
Packaging error in which customers who ordered product code 140880 (verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (verres cannula with integral needle tip).
조치
Teleflex sent an Medical Device Advisory Notification letter dated January 8, 2016, to all affected customers notifying them of the packaging error.
Our records indicate that you have received products that are subject to this notification.
Teleflex Medical is committed to providing high quality, safe and effective products. We sincerely apologize for any inconvenience this action may cause your operations. If you have any other questions, feel free to contact your local sales representative or Customer Service at recalls@teleflex.com or 1-866-246-6990.