Overview of high-risk medical device recalls in obstetrics and gynecology from 2002 through 2016: implications for device safety.
PMID: 28500861 ·
T, i, m, o, t, h, y, , M, , J, a, n, e, t, o, s, ;, , C, o, m, e, r, o, n, , W, , G, h, o, b, a, d, i, ;, , S, h, u, a, i, , X, u, ;, , J, e, s, s, i, c, a, , R, , W, a, l, t, e, r
Publicidad
Resumen
The field of women's health has endured numerous recent controversies involving medical devices such as pelvic meshes, laparoscopic morcellators, and a hysteroscopic sterilization device. With the recent passage of the 21st Century Cures Act, new legislation will change how the Food and Drug Administration regulates medical devices. Given these controversies and new changes, we investigated high-risk, class I recalls in women's health from 2002 through 2016. Class I recalls for medical devices a
Publicidad
Fuente oficial
Ver en PubMed →Datos obtenidos de PubMed / NCBI. Para consultar el texto completo y la información más reciente, remítase siempre al registro oficial.