FDA Class II Recall: PURPREP by CareFusion 213, LLC — Recall Details

Key facts

What consumers should do

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Specifically, check whether the product in your possession matches the description on file with FDA -- BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL Applicators per carton. Carefusion 213 LLC, El Paso, TX 79912, NDC 54365-014-42. -- and the recall number D-0517-2026. If it matches, stop using or distributing it and contact CareFusion 213, LLC or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice.

What this classification means

FDA classifies a recall as Class II when using the recalled product, or being exposed to it, may cause temporary or medically reversible adverse health consequences, or when the probability of serious adverse health consequences is remote. In this case, the recalling firm is CareFusion 213, LLC and the affected product is described in FDA's record as: BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL Applicators per carton. Carefusion 213 LLC, El Paso, TX 79912, NDC 54365-014-42.. FDA's stated reason for the recall is: Lack of assurance of Sterility: potential product contamination. The recall is tracked under FDA recall number D-0517-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended. Adverse events believed to be related to a recalled product can be reported to FDA's MedWatch program, which FDA uses to monitor safety signals after a recall is opened.

CareFusion 213, LLC’s FDA history

Argus HQ has recorded 7 total FDA actions tied to CareFusion 213, LLC: 1 warning letter, 6 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

What should someone who has this product do?

Because this recall carries FDA's middle severity classification, anyone who has this product should stop using it and follow the recalling firm's instructions, even though serious harm is considered unlikely for this classification. Check the product against FDA's description (BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL Applicators per carton. Carefusion 213 LLC, El Paso, TX 79912, NDC 54365-014-42.) and recall number D-0517-2026, then follow CareFusion 213, LLC's recall instructions.

Has CareFusion 213, LLC had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 7 total FDA actions tied to CareFusion 213, LLC, including 6 recalls and 1 warning letter.

What is the FDA recall number for this event?

FDA recall number D-0517-2026.

What is the current status of this recall?

Status as recorded by FDA: Ongoing.

Related enforcement actions

• Warning letter: CareFusion 213, LLC — CGMP/Finished Pharmaceuticals/Adulterated (2026-04-30) →