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FDA · Drugs ·

BD PurPrep recall

CareFusion 213, LLC recalled BD PurPrep on May 13, 2026 because of lack of assurance of Sterility: potential product contamination. It was sold nationwide.

Why it was recalled

Lack of assurance of Sterility: potential product contamination

What's recalled

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

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice