Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TRIMIX FORTE 30MG/2MG/20MCG/ML INJ in 1 mL vial Assurance Infusion Recalled by Assurance Infusion Due to Lack of sterility assurance.
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 Assurance Infusion directly.
Affected Products
TRIMIX FORTE 30MG/2MG/20MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
Quantity: 358 vials
Why Was This Recalled?
Lack of sterility assurance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Assurance Infusion
Assurance Infusion has 118 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report