Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
BIOPHEN UFH Control Plasma Recalled by Aniara Diagnostica LLC Due to Incorrect product labeling was included in the package.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aniara Diagnostica LLC directly.
Affected Products
BIOPHEN UFH Control Plasma
Quantity: 13 units (1 unit is 1 box)
Why Was This Recalled?
Incorrect product labeling was included in the package.
Where Was This Sold?
This product was distributed to 2 states: IL, MI
About Aniara Diagnostica LLC
Aniara Diagnostica LLC has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report