CareFusion BD PurPrep Sterile Solution Recall: Potential Contamination Risk

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Contact the company & request your remedy

Recalling firmCareFusion 213, LLC1550 Northwestern Dr · El Paso, TX 79912-8000

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

CareFusion is recalling BD PurPrep povidone-iodine solution because it may be contaminated. This could lead to infections if used improperly. The recall affects specific lots with expiration dates through October 2026.

Why it’s dangerous

The solution may not be sterile, which could lead to infections if used on open wounds or skin. Contamination can occur during manufacturing or storage, especially if the product is not handled properly.

Who’s affected

People who own or use BD PurPrep povidone-iodine solution for medical purposes are affected. Those using the product for wound care or disinfection are at higher risk.

How to tell if you have this one

Check the product label for the lot numbers: 4258309, 4260329, 4256875 (expiring August 2026), 4296453, 4317319, 4290654 (September 2026), and 4322449, 4323861, 4318679 (October 2026). The product comes in 25x26mL applicators per carton.

Brand
CareFusion
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Lot Number
Look for lot numbers on the label: 4258309, 4260329, 4256875 (expiring August 2026), 4296453, 4317319, 4290654 (September 2026), or 4322449, 4323861, 4318679 (October 2026).

✎ GovInfoNow

Questions people ask

What is the product being recalled?

BD PurPrep povidone-iodine 8.3% w/w with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL applicators per carton.

What is the hazard?

Potential product contamination, which could lead to infections if used on open wounds or skin.

How can I tell if I have the recalled product?

Check the lot numbers on the label: 4258309, 4260329, 4256875 (expiring August 2026), 4296453, 4317319, 4290654 (September 2026), or 4322449, 4323861, 4318679 (October 2026).

Take action

Contact CareFusion

We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0517-2026 — CareFusion CareFusion

Hello,

I own a CareFusion that is covered by recall D-0517-2026 from CareFusion.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0517-2026 (April 22, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0517-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

CareFusion 213, LLC recalls BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution,

Recall notice