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 skin wipes for the bioderm liberty 3.0 external male catheter, bioderm liberty pouch clean & dry external male catheter and bioderm safe n' dry. this component (wipes) were initially manufacturer by smith & nephew and recalled due to a potential bacterial contamination.
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 Liberty 3.0 External Male Catheter Specialty Type with integral collection chamber (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.