The Food and Drug Administration admitted Thursday that it mistakenly approved a patch for injured knees last year after being pressured by members of Congress and the manufacturer.
Internal documents demonstrate that agency’s scientific reviewers repeatedly determined that the device, known as Menaflex and manufactured by ReGen Biologics Inc., was unsafe because the device often failed, forcing patients to get another operation.
New research makes the case for educating women in their 40s — who've been caught in...
Second gentleman Doug Emhoff tested positive for COVD-19, the vice president’s office announced Sunday.
His office said...
