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Aniara Diagnostica LLC recalls BIOPHEN UFH Control Plasma
Recalled September 21, 2022 · FDA recall Z-1743-2022 · Aniara Diagnostica
Hazard
Incorrect product labeling was included in the package. · FDA Class III
Units
13 units (1 unit is 1 box)
Sold at
Distribution in US - IL and MI
Description
Incorrect product labeling was included in the package.
Product
BIOPHEN UFH Control Plasma
Manufacturer(s)
Aniara Diagnostica LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →