We use cookies to ensure the website works properly and to improve your experience. By continuing to use the website, you agree to their use.
Для размещения заказа оставьте ваш номер телефона. Мы с вами свяжемся в ближайшее время
Regulatory information
Recall Notice: Rapid Bio HIV Ag/Ab Combo Rapid Test, Kit No. 4
Dear Users,
Rapid Bio LLC hereby announces the recall of Kit No. 4 of the medical device "RAPID HIV AG/AT IHA" (Registration Certificate No. РЗН 2024/22068 dated June 19, 2025).
Reason for Recall
Letter No. 01i-284/26 dated April 2, 2026, from the Federal Service for Surveillance in Healthcare (Roszdravnadzor) regarding the suspension of use of the medical device due to a potential risk of harm to the life and health of citizens.
Detailed information regarding this notice is provided in the attached file
