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 […]
FDA Advisory No.2023-0051-A || Lifting of the FDA Advisory No. 2023-0051 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product ProCare Adult Diapers”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, ProCare Adult Diapers, has been issued an FDA Certificate of Medical […]
FDA Advisory No.2022-0107-A || Lifting of the FDA Advisory No. 2022-0107 entitled “Reiteration on Prohibition of Online Selling of FDA Certified COVID-19 Test Kits including Self-Administered COVID-19 Test Kits”
In line with the Department of Health Department Memorandum (DM) No. 2022-0033 entitled “Guidelines on the Use of Self-Administered Antigen Testing for COVID-19, the Food and Drug Administration (FDA) informs […]
FDA Advisory No.2022-1815-A || Lifting of the FDA Advisory No. 2022-1815 entitled Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “ Pro Health Care Nasal Oxygen Cannula”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Pro Health Care Nasal Oxygen Cannula, has been issued an FDA […]
FDA Advisory No.2022-0017-A || Lifting of the FDA Advisory No. 2022-0017 entitled Public Health Warning Against the Purchase and Use of the Uncertified Self-Administered COVID-19 Test Kit “ ARIA SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold Immunochromatography)”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, Uncertified Self-Administered COVID-19 Test Kit “ARIA SARS-CoV-2 Antigen Rapid Test Kit […]
FDA Advisory No.2022-1586-A || Lifting of the FDA Advisory No. 2022-1586 entitled “Public Health Warning Against the Purchase and Use of the Following Unnotified Medical Device Products:
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that Outshine Philippines Inc., the distributor of Med Guard Cotton Balls and Med Guard Pure and […]
FDA Advisory No.2022-1578-A || Lifting of the FDA Advisory No. 2022-1578 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “MED GUARD® COTTON BUDS”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the Outshine Philippines, Inc., the distributor of MED GUARD® COTTON BUDS, had complied with the […]
FDA Advisory No.2022-1673-A || Lifting of the FDA Advisory No. 2022-1673 entitled Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “SM BONUS UNDERPADS”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, SM Bonus Underpads, has been issued an FDA Certificate of Medical […]
FDA Advisory No.2021-0400-A || Lifting of the FDA Advisory No. 2021-0400 entitled “Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product ICARE® DISPOSABLE FACE MASK”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product, ICARE® DISPOSABLE FACE MASK, has been issued an FDA Certificate of […]
FDA Advisory No.2022-1523-A || Lifting of the FDA Advisory No. 2022-1523 entitled “Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “INDOPLAS ELITE TOKYO JAPAN DIGITAL THERMOMETER”
The Food and Drug Administration (FDA) informs all healthcare professionals and the general public that the medical device product stated on FDA Advisory No. 2022-1523, “Indoplas Elite Tokyo Japan Digital […]