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
Bandage, liquid, skin protectant - Product Code NEC
원인
On 06/08/2011, bioderm, inc. issued a voluntary recall of a component (smith and nephew skin wipes) used in the bioderm liberty 3.0 external male catheter, bioderm liberty pouch clean & dry external male catheter and bioderm safe n' dry. potential bacterial contamination of smith and nephew skin wipes by one of their contract manufacturers.
조치
Notice was sent to customers by letter dated June 8, 2011 and by phone.
Worldwide Distribution-USA (nationwide) including the states of AZ, CA, FL, NH, NJ, NY, PA, TX, and WI, and the countries of Canada and Netherlands.
제품 설명
BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). || The recalled wipes are used on intact skin for applying skin protectant to the glands for control of male incontinence with an external, non-invasive and nonsterile device.