QUADMIX FORTE in 1 mL vial Assurance Infusion (713) 533-8800
FDA Recall #D-0765-2020 — Class II — December 20, 2019
Product Description
QUADMIX FORTE in 1 mL vial Assurance Infusion (713) 533-8800
Reason for Recall
Lack of sterility assurance.
Recalling Firm
Assurance Infusion — Houston, TX
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
5 vials
Distribution
Nationwide within the United States
Code Information
Lot: 08132019@15 Exp. 02/09/2020
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated