BD recalls ChloraPrep Clear antiseptic applicators that were distributed without proper sterilization, potentially causing infections if used on open wounds.
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 Clear antiseptic applicators that were distributed without proper sterilization. Using these unsterilized items could lead to infections if they come into contact with open wounds.
The applicators were distributed outside their intended use for sterilization, meaning they may not be sterile. If used on open wounds, this could introduce bacteria and cause infections.
Healthcare professionals and patients using these antiseptic applicators for wound care. Those with open wounds are at higher risk of infection.
Check for BD ChloraPrep Clear applicators with NDC 54365-400-32. Look for specific lot numbers listed in the recall notice, such as 3214024 or 4030693.
Look for the lot number on the packaging, which is listed in the recall notice (e.g., 3214024, 4030693).
Reach out to BD Customer Support for specific instructions on whether to discard or return the product.
The applicators were distributed without proper sterilization, meaning they may not be sterile and could cause infections if used on open wounds.
Check for BD ChloraPrep Clear applicators with NDC 54365-400-32 and specific lot numbers listed in the recall notice.
The recall does not require immediate discontinuation; contact BD for guidance on whether to discard or return the product.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall D-0645-2026 — BD BD Hello, I own a BD that is covered by recall D-0645-2026 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.
