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
bone graft preparation syringe - Product Code FMF
원인
The syringe assembly has an obstruction in the tube that prevents the plunger from being depressed.
조치
Consignees were notified by letter dated either 6/11/07 or 6/13/07 and requested to return the product.
Worldwide, including USA, Chile, Italy, Spain and United Kingdom.
제품 설명
Vortech Graft Preparation System, sterile, single use, disposable, Distributed by Biomet Biologics, Inc., Warsaw, Indiana; REF 800-0300V. (Not sold in the United States).