BD ChloraPrep Scrub Teal (2% chlorhexidine gluconate and 70% isopropyl alcohol) with unsterilized applicators may cause infections. Recalled lots from 2026-2028; contact BD for details.
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
BD ChloraPrep Scrub Teal products with unsterilized applicators were recalled because they were distributed outside their intended use. Using these products could lead to infections if not properly sterilized.
The applicators were distributed without proper sterilization, meaning they could be contaminated. This poses a risk of infection if used in medical procedures where sterility is critical.
Healthcare professionals and surgical staff who use these products for sterilization or cleaning. Those handling the recalled lots are at risk of infection.
Check for BD ChloraPrep Scrub Teal with 100 x 10.5 mL applicators. Look for lot numbers like 4157798 (expiring 05/31/2027) or 3330777 (expiring 10/31/2026).
Look for lot numbers on the packaging, such as 4157798 or 3330777, which are associated with the recalled products.
Reach out to BD CareFusion for specific instructions on whether your product is affected and what to do next.
The applicators were distributed without proper sterilization, meaning they could be contaminated and pose an infection risk during medical procedures.
Check the lot number on your packaging. If it matches the recalled lots, contact BD CareFusion for instructions on how to handle the product.
Yes, using unsterilized applicators could lead to infections, especially in medical procedures where sterility is critical.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall D-0649-2026 — BD BD Hello, I own a BD that is covered by recall D-0649-2026 from BD. 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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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.
