FDA Advisory No.2023-1946-A|| Lifting of the FDA Advisory No. 2023-1946 entitled Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “ICARE® INFRARED THERMOMETER”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, iCARE® Infrared Thermometer, has been issued an FDA Certificate of Medical […]
FDA Advisory No.2022-1909-A || Lifting of the FDA Advisory No. 2022-1909 entitled Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “Mr. DIY Reading Glasses”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Unnotified Mr. DIY Reading Glass, has been issued an FDA Certificate […]
FDA Advisory No.2022-1544-A || Lifting of the FDA Advisory No. 2022-1544 entitled Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “Mr. DIY Reading Glasses”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Unnotified Mr. DIY Reading Glass, has been issued an FDA Certificate […]
FDA Advisory No.2023-2187-A || Lifting of the FDA Advisory No. 2023-2187 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “PARA AID ICE BAG”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Para Aid Ice Bag has been notified by the Market Authorization […]
FDA Advisory No.2023-2186-A || Lifting of the FDA Advisory No. 2023-2186 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “INDOPLAS DIAGNOSTIC LAMP”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Indoplas Diagnostic Lamp has been notified by the Market Authorization Holder […]
FDA Advisory No.2023-1765-A || Lifting of the FDA Advisory No. 2022-1765 entitled “Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product TOP CARE AUTOMATIC LANCING DEVICE”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Unregistered Top Care Automatic Lancing Device, has been issued a proper […]
FDA Advisory No.2023-0014-A || Lifting of the FDA Advisory No. 2022-0014 entitled “Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “IZUMI BIO-STREAM 4 STAGES DRINKING WATER SYSTEM”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the water purification device/system, Izumi Bio-Stream 4 Stages Drinking Water has been registered by the […]
FDA Advisory No.2023-0207-A || Lifting of the FDA Advisory No. 2023-0207 entitled “Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product ICARE® NEBULIZER KIT WITH PEDIATRIC AEROSOL MASK (NM06-002, 12ML)”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, iCare® Nebulizer Kit with Pediatric Aerosol Mask (NM06-002, 12mL) has been […]
FDA Advisory No.2023-0669-A || Lifting of the FDA Advisory No. 2023-0669 entitled Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “ Promisemed Blood Lancet ”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Unregistered Promisemed Blood Lancet, has been issued an FDA Certificate of […]
FDA Advisory No.2023-1811-A || Lifting the Advisory of the following Medical Device Products under FDA Advisory No. 2020-1811 entitled “Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Products”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the advisory on the following medical device products under FDA Advisory No. 2020-1811 dated 05 […]