Recall
FDAHealthApril 22, 2026

CareFusion 213, LLC — BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213,

⚠️ Lack of assurance of Sterility: potential product contamination

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 22, 2026

Nationwide in the USA

What's affected?

Product
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl. oz. (10.5 mL) x 25 applicators per box. Carefusion 213, LLC, El Paso, TX 79912, subsidary of Becton Dickinson and Co. NDC 54365-014-41
Brand
PURPREP
Lot code
#

Additional details

Lots# 4263873, Exp. Date 08-31-2026, 4320590, Exp. Date 09-30-2026, 4320591, Exp. Date 10-31-2026.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated

View original FDA notice →

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