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
Sharps Needle Destruction Device - Product Code MTV
원인
Their needlezap devices were not manufactured in accordance with the quality system regulations, and were shipped without an approved pma.
조치
On 8/15/2002, the firm contacted their largest distributor by telephone and instructed them to stop distribution and to place all remaining devices in quarantine until further notice. On 3/20/2003, the firm mailed recall notices to all direct accounts asking for the device to be returned.
The devices were shipped to customers located nationwide. The product was also distributed into Canada, Greece and Ireland.
제품 설명
NEEDLEZAP, a battery operated needle destruction device. || The product is labeled and marketed for use only in the law enforcement market or veterinary market.