The product, BM-3000, sold from June 15, 2011 to October 5, 2011 has been ordered to be withdrew by the Food and Drug Administration, as it was found to be a medical equipment with no permit.
Subject of the withdrawal: BM-300 (sold from June 15, 2011 to October 5, 2011)
Cause of the withdrawal: Violation of 25th provision of the medical equipment law.
For those of you, customers, who have a possession of this product, please contact our company and we will arrange a solution promptly.
For a reference, the product that was sold during the period has a KGMP mark on the top right on the first pace of the manual. For those who apply, please contact us. Thank you.