D-1359-2014 Class II Terminated

Recalled by Carefusion 2200 Inc — Vernon Hills, IL

FDA drug recall D-1359-2014 was initiated by Carefusion 2200 Inc on Dec 20, 2013 and is designated Class II. Reason for recall: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner. The available iodine in the product is less than as stated on the product label. The recall status is terminated (terminated Jun 11, 2015). Affected quantity: 2,443,500 scrub brushes.

Recall Details

Product Type
Drugs
Report Date
Jun 11, 2014
Initiation Date
Dec 20, 2013
Termination Date
Jun 11, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2,443,500 scrub brushes

Product Description

CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9% Povidone-iodine (USP) Surgical Hand Scrub; CareFusion, Vernon Hills, IL 60061 USA, NDC 57613-003-18

Reason for Recall

Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner. The available iodine in the product is less than as stated on the product label.

Distribution Pattern

Nationwide and Puerto Rico; Bahrain, Germany, Mexico, Philippines

Code Information

4451B; 4451GL

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-1359-2014
openFDA file date
Oct 27, 2026
Loaded by RegDataLab
Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.