Drug Enforcement D-1102-2023

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Status

Completed

Classification

Class II

Report Date

August 30, 2023

Termination Date

Product Information

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.
Product quantity
38,486 vials
Reason for recall
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Recall initiation reason
Initial firm notification
Letter
Distribution pattern
Nationwide in the USA

Location & Firm

Recalling firm
Ecometics, Inc.
Address
19 Concord St, N/A

United States
Voluntary / Mandated
Voluntary: Firm initiated
Status date

Codes & Dates

Recall number
D-1102-2023
Event ID
92857
Recall initiation date
August 9, 2023
Center classification date
August 24, 2023
Code info
Lot #: 2E235A, exp: 2/2024; 2E293A, exp: 3/2024
More code info