CareFusion 213, LLC: BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available
Recall reason: Lack of assurance of Sterility: potential product contamination. Recalled by CareFusion 213, LLC. Distribution: Nationwide in the USA. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot# 4258309, 4260329, 4256875, Exp. Date, 08-31-2026; 4296453, 4317319, 4290654, Exp. Date 09-30-2026; 4322449, 432. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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