FDA Advisory No.2022-0002-A || Lifting of the FDA Advisory No. 2022-0002 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product NOSK NASAL FILTER”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, NOSK NASAL FILTER, has been notified by the Market Authorization Holder […]
FDA Advisory No.2021-2452-A || Lifting the Advisory of NADAL COVID-19 Ag Test under FDA Advisory No. 2021-2452 entitled: Caution on the purchase and use of certain COVID-19 Test Kits following the performance validation conducted by the RITM
The Food and Drug Administration (FDA) informs all healthcare professionals and general public that the advisory on NADAL COVID-19 Ag Test manufactured by Nal Von Minden GmbH under FDA Advisory […]
FDA Advisory No.2021-2704-A || Lifting of the FDA Advisory No. 2021-2704 entitled “Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product MEDICA® FLEXIBLE DIGITAL THERMOMETER WITH FLEXIBLE TIP”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, MEDICA® FLEXIBLE DIGITAL THERMOMETER WITH FLEXIBLE TIP, has been issued an […]
FDA Advisory No.2021-1893-A || Lifting of the FDA Advisory No. 2021 -1893 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product LIGHT/WASH CHROMACLONE® PVS FAST SET BUBBLE GUM FLAVOR”
The Food and Drug Administration (FDA) informs all healthcare professionals and general public that the medical device product LIGHT/WASH CHROMACLONE® PVS FAST SET BUBBLE GUM FLAVOR has been notified by […]
FDA Advisory No.2021-2363-A || Lifting the Advisory of Alpk2 Aneroid Sphygmomanometer under FDA Advisory No. 2021-2363 entitled Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product ANEROID SPHYGMOMANOMETERS
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product Alpk2 Aneroid Sphygmomanometer has been issued a FDA Certificate of Exemption […]
FDA Advisory No.2021-1678-A || Lifting of the FDA Advisory No. 2021-1678 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product Long Bone Plaster of Paris Bandage (6” x 5y )”
The Food and Drug Administration (FDA) informs all healthcare professionals and general public that the medical device product Long Bone Plaster of Paris Bandage (6” x 5y) has been registered […]
FDA Advisory No.2019-525-A || Lifting the Advisory of the Registered Medical Device under FDA Advisory No. 2019-525 entitled Public Health Warning Against the Purchase and Use of the Unregistered Medical Device “SURGITECH CLINICAL FIEBER THERMOMETER MT-101
The Food and Drug Administration (FDA) informs all healthcare professionals and the public that the medical device product “Surgitech Clinical Fieber Thermometer MT-101” has been registered by the Market Authorization […]
FDA Advisory No.2020-782-A || Lifting the Advisory of the Notified Medical Device under FDA Advisory No. 2020-782 entitled Public Health Warning Against the Unapproved and Misleading Health Claims of Medical Devices that Decreases the Risk for Coronavirus Disease (COVID-19) Infection
The Food and Drug Administration (FDA) informs all healthcare professionals and the public that the medical device product “Respokare® Active Protection Mask Anti-Viral Mask” has been notified by the Market […]
FDA Advisory No.2020-1809-A || Lifting of the FDA Advisory No. 2020-1809 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product i-shield GAUZE PAD sterilized (4” x 4” x 8 ply 28 x 24 mesh)”
The Food and Drug Administration (FDA) informs all healthcare professionals and general public that the medical device product i-shield GAUZE PAD sterilized (4” x 4” x 8 ply 28 x […]
FDA Advisory No.2020-1973-A || Lifting of the Advisory No. 2020-1973 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “SURGITECH FACE MASK (SURGICAL DISPOSABLE 3PLY 50PCS)”
The Food and Drug Administration (FDA) informs all healthcare professional and the general public that the medical device product Surgitech Face Mask (Surgical Disposable 3Ply 50 pcs), has been notified […]