Medline recalls convenience kits with BD ChloraPrep Clear 1mL applicators due to potential open seals causing sterility breaches. Affected kits may lead to patient infections if used.
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 ChloraPrep Clear 1mL applicators labeled for C-SECTION PREP. The recall is because these applicators might have open seals, which could breach sterility and cause infections.
The applicators may have open seals on their packaging, which can breach sterility. This breach could lead to infections for patients during medical procedures.
Healthcare workers using these kits for surgical prep are most at risk. Patients receiving the procedure may face infection if the applicator is not sterile.
Check for kits labeled 'C-SECTION PREP' with reference number DYNJ32702B. Lot numbers 24EBR761 are included in the affected batch.
Look for the label 'C-SECTION PREP' and reference number DYNJ32702B on the kit.
The applicators may have open seals on their packaging, which can breach sterility and lead to infection risks for patients.
The recall record does not specify a remedy, so check with Medline directly for instructions.
Look for kits labeled 'C-SECTION PREP' with reference number DYNJ32702B and lot number 24EBR761.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2156-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2156-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
