CareFusion 213, LLC Recalls

2 recalls found for CareFusion 213, LLC — April 2026.

Medications: 2

The recalls listed below are active notices associated with CareFusion 213, LLC in the FDA, NHTSA, USDA, and CPSC databases. None of the current recalls are classified as urgent. The current recalls involve sterility concerns. Check the specific lot numbers, model numbers, or production date codes in each notice carefully — a recall typically covers specific production runs, not everything a manufacturer sells.

A manufacturer appearing in the recall database does not indicate an ongoing safety failure. High-volume companies with large product lines naturally appear more frequently. What matters is whether your specific product — identified by lot number, model number, or date code — is included in a recall notice.

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NoticeMedications

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl

CareFusion 213, LLC

Lack of assurance of Sterility: potential product contamination

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NoticeMedications

BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL

CareFusion 213, LLC

Lack of assurance of Sterility: potential product contamination

View recall →