FDA Revokes Emergency Use Authorization for Blood Filter Manufactured by ExThera Medical
February 19, 2026
February 19, 2026
WASHINGTON, Feb. 19 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration has revoked of the emergency use authorization (EUA) for the Seraph 100 Microbind Affinity blood filter manufactured by ExThera Medical Corp., Martinez, California. The decision follows a request from the company to withdraw the authorization for the device.
The original EUA was issued on April 17, 2020, to bolster public health protections during the pandemic. Under section . . .
The original EUA was issued on April 17, 2020, to bolster public health protections during the pandemic. Under section . . .