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
Gynecologic laparoscope and accessories - Product Code HET
원인
There is the potential for the duckbill seal to become dislodged.
조치
Recall notification letters titled "URGENT VOLUNTARY PRODUCT RECALL" were sent on 10/8/2009 via UPS next day. The letters describe the lots within expiration that are recalled. The motor drive unit is not included in the recall. Letters have photos and illustrations of the product which clearly show the location of the product code and expiration date. Recalled product is to be returned to Stericyle using an enclosed pre-paid authorized shipping label. Ethicon will notify customers when the product is available.
Questions are to be directed to Ethicon at 1-888-276-5901.
Worldwide distribution - US and United Arab Emirates, Argentina, Austria, Australia, Belgium, Brazil, Canada, Switzerland, China, Czech Republic, Germany, Denmark, Egypt, Spain, Finland, France, United Kingdom, Greece, Israel, Italy, Jordan, Republic of Korea, Mexico, Malaysia, Netherlands, Norway, New Zealand, Puerto Rico, Reunion, Russian Federation, Sweden, Slovina, Turkey, Saudi Arabia, Venezuela and S. Africa.
제품 설명
Gynecare Morcellex Tissue Morcellator; || Manufactured by: Ethicon Women's Health & Urology; || A Division of ETHICON INC, a Johnson & Johnson Company, Somerville, NJ 08876