Public Alert No.024/2021 – Boston Scientific Corporation Recalls VICI VENOUS STENT System and VICI RDS VENOUS STENT System for Potential of Stent Migration
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by the U.S Food and Drug Administration (FDA) that Boston Scientific is recalling the VICI VENOUS STENT System (VICI SDS) and RDS VENOUS STENT Systems after reports indicate that the stents may migrate or move from where they are initially […]
Public Alert No.023/2021 – Miracle8989 Issues Voluntary Nationwide Recall of PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000, Due to Presence of Undeclared Sildenafil and Tadalafil
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by the U.S Food and Drug Administration that Irving, Texas, Miracle8989 is voluntarily recalling all lots of PremierZen Gold 7000, PremierZen Platinum 8000 and MaxxZEN Platinum 12000, capsules to the consumer level. FDA analysis has found the products to contain […]
Public Alert No.022/2021 – Update: FDA Recommends Transition from Use of Non-NIOSH-Approved and Decontaminated Disposable Respirators – Letter to Health Care Personnel and Facilities
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed that the U.S. Food and Drug Administration (FDA) is recommending health care personnel and facilities to transition away from crisis capacity conservation strategies, such as using non-NIOSH-approved disposable respirators, including non-NIOSH-approved imported respirators such as KN95s. This recommendation is in […]
