FDA Advisory No.2024-0029 || Public Health Warning Against the Purchase and Use of the Unnotified Medical Device Product “ELDERJOY ADULT SLIM PANTS”
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. ELDERJOY ADULT SLIM PANTS The […]
FDA Advisory No.2024-0008 || Public Health Warning Against the Purchase and Use of the Unregistered Medical Device “ACCUFAST 99.99 RAPID CHECK PREGNANCY TEST”
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. ACCUFAST 99.99 RAPID CHECK PREGNANCY […]
FDA Advisory No.2024-0009 || Revision in the Process of Application for Certificate of Medical Device Registration (CMDR)/Certificate of Medical Device Notification (CMDN), Initial and Renewal
In line with the Food and Drug Administration’s objective to improve the processing of CMDR initial and CMDR/CMDN renewal applications, a revision in the process is being implemented. For all […]
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 […]