Medline recalls convenience kits with BD ChloraPrep Clear 1mL applicators that may have open packaging, risking sterility breaches and patient infections. Affected kits include specific blood culture kit references and lot numbers.
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 containing BD ChloraPrep Clear 1mL applicators that were previously recalled by BD for potential open packaging. This could breach sterility and lead to patient infections if used.
The applicators may have an open seal on their packaging, which could breach sterility. This breach might lead to infections for patients during medical procedures.
Healthcare professionals using blood culture kits with specific references and lot numbers. Patients receiving procedures using these kits are at risk of infection.
Check for kits labeled as blood culture kits with references DYNDH1462B, DYNDH1622C, or DYNDH1866. Look for lot numbers 24EBU164, 24FBD281, 24FBK195, 24EBU004, or 24EBT285.
Look for kit references DYNDH1462B, DYNDH1622C, or DYNDH1866 and associated lot numbers to confirm if your kit is affected.
BD previously recalled these applicators due to potential open packaging, which could breach sterility and lead to patient infections.
Check for kit references DYNDH1462B, DYNDH1622C, or DYNDH1866 and lot numbers 24EBU164, 24FBD281, 24FBK195, 24EBU004, or 24EBT285.
The recall does not require immediate stop use; affected kits should be checked for the specific references and lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2155-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2155-2025 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.
