BD recalls ChloraPrep Hi-Lite Orange applicators due to unsterilized distribution. These items may cause infections if used without proper sterilization.
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 is recalling ChloraPrep Hi-Lite Orange antiseptic solutions because some applicators were distributed without proper sterilization. Using these unsterilized items could lead to infections if not properly cleaned or sterilized before use.
The applicators were distributed outside their intended sterilization channel, meaning they were not properly sterilized. This increases the risk of infection when used on wounds or skin without adequate cleaning.
Healthcare professionals and patients using the ChloraPrep Hi-Lite Orange antiseptic solutions for wound care. Those who have used the recalled applicators without proper sterilization are at risk of infection.
Check for BD ChloraPrep Hi-Lite Orange (2% chlorhexidine gluconate and 70% isopropyl alcohol) packaged as 100 x 3mL or 250 x 3mL applicators. Look for specific lot numbers and expiration dates listed in the recall notice.
Identify the product by checking the lot number and expiration date on the packaging.
If you have the recalled product, stop using it immediately to prevent infection risks.
The applicators were distributed without proper sterilization, increasing the risk of infection if used without adequate cleaning.
Stop using it immediately and check the product details to confirm if it's recalled.
Yes, using unsterilized applicators could lead to infections if not properly cleaned or sterilized before use.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall D-0647-2026 — BD BD Hello, I own a BD that is covered by recall D-0647-2026 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.
