Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm...
FDA Recall #D-1102-2023 — Class II — August 9, 2023
Product Description
Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6064-0, Ref 6064.
Reason for Recall
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Recalling Firm
Ecometics, Inc. — Norwalk, CT
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
38,486 vials
Distribution
Nationwide in the USA
Code Information
Lot #: 2E235A, exp: 2/2024; 2E293A, exp: 3/2024
Status
Completed
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.