Becton Dickinson & Company has recalled approximately 628,000 units of ChloraPrep OneStep (2% chlorhexidine gluconate and 70% isopropyl alcohol) 3 mL applicators. The recall was initiated because the products are incorrectly labeled as the "Clear" version when they actually contain the "Hi Lite Orange" tinted version. While the medication itself is the same, this labeling error could lead to confusion during surgical preparation where a clear or tinted solution is specifically required. Consumers should contact their healthcare provider or pharmacist regarding any unused applicators from the affected lot.
The labeling mixup means medical professionals may unknowingly apply a tinted orange solution instead of a clear one, which could interfere with site visibility or patient expectations during clinical procedures. No injuries or adverse events have been reported due to this specific label error.
Product return and refund
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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