Medline recalls convenience kits with BD ChloraPrep Clear 1mL applicators due to potential open packaging that could breach sterility, risking patient infection.
Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its packaging. This may constitute a breach to sterility, which may in turn lead to the infection related harms for the patient.
Medline is recalling convenience kits that include BD ChloraPre: 1mL applicators because the packaging might have an open seal. This could lead to contamination and infection for patients during medical procedures.
The packaging of the BD ChloraPrep Clear 1mL applicators might have an open seal, which could breach sterility. This breach might allow contamination, potentially leading to infections for patients during medical procedures.
Healthcare workers using these kits for medical procedures are most at risk. Patients receiving care with the recalled kits could face infection if the packaging is compromised.
Check for kits labeled 'IV START KIT LAB DRAW-SH, REF CDS860014P' with lot numbers 24EBR549. The kits were sold with UDI/DI numbers 10888277797819 (each unit) and 40888277797810 (case).
Look for the label 'IV START KIT LAB DRAW-SH, REF CDS860014P' and lot number 24EBR549 on the kit.
The packaging of the BD ChloraPrep Clear 1mL applicators might have an open seal, which could breach sterility and lead to patient infections.
Check for kits labeled 'IV START KIT LAB DRAW-SH, REF CDS860014P' with lot number 24EBR549.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2154-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2154-2025 from Medline. 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.
