FDA Advisory No.2023-2575 || Public Health Warning Against the Purchase and Use of the Following Unnotified Medical Device Products:
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unnotified medical device products: 1. “MEDX KNEE SUPPORT PATELLA” 2. […]
FDA Advisory No.2023-2574 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “MTI-FRANCE DIAGNOSTIC LAMP”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unnotified medical device product: 1. MTI-FRANCE DIAGNOSTIC LAMP The FDA […]
FDA Advisory No.2023-2573 || Public Health Warning Against the Purchase and Use of the Following Unnotified “MEDX” Medical Device Products:
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the following unnotified medical device products: 1. MEDX” Medical Device Products […]
FDA Advisory No.2023-2537 || APPLICATION HOLIDAY FOR CERTIFICATE OF MEDICAL DEVICE NOTIFICATION (CMDN) APPLICATIONS
The Center for Device Regulation, Radiation Health, and Research (CDRRHR) of the Food and Drug Administration (FDA) will be conducting an inventory and processing of the pending applications for registration […]
FDA Advisory No.2023-2387 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “PRIME TRANS TRANSPARENT MICROPERFORATED HYPOALLERGENIC TAPE”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unnotified medical device product: 1. PRIME TRANS TRANSPARENT MICROPERFORATED HYPOALLERGENIC […]
FDA Advisory No.2023-2275 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “RESQ™ UNDERPADS”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unnotified medical device product: 1. RESQ™ UNDERPADS The FDA verified […]
FDA Advisory No.2023-2281 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “PRIME POR HYPOALLERGENIC MICROPOROUS SURGICAL TAPE”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unnotified medical device product: 1. PRIME POR HYPOALLERGENIC MICROPOROUS SURGICAL […]
FDA Advisory No.2023-2280 || Public Health Warning Against the Purchase and Use of the Unregistered Medical Device “SOLITAIRE NASAL OXYGEN CANNULA”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unregistered medical device product: 1. SOLITAIRE NASAL OXYGEN CANNULA The […]
FDA Advisory No.2023-2274 || Public Health Warning Against the Purchase and Use of the Unregistered Medical Device Product “MAXI EYES™ SPECTROFLEX COLORS LENS”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unregistered medical device product: 1. MAXI EYES™ SPECTROFLEX COLORS LENS […]
FDA Advisory No.2023-2279 || Public Health Warning Against the Purchase and Use of the Following Unnotified Medical Device Products “GLAN CURE TINYTAN COOLING GEL SHEET (IN FOREIGN CHARACTERS)”
The Food and Drug Administration (FDA) warns all healthcare professionals and the general public NOT TO PURCHASE AND USE the unnotified medical device products: 1. GLAN CURE TINYTAN COOLING GEL […]