Medline recalls Labor Triage Kits with BD ChloraPrep Clear applicators due to potential open packaging that could breach sterility, risking infection. Affected kits have specific lot numbers and reference codes.
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 Labor Triage Kits that contain BD ChloraPre: 1mL applicators because the packaging might have an open seal, which could lead to infection if used improperly. This is a serious risk for patients during medical procedures.
The BD ChloraPrep Clear applicators may have an open seal in their packaging, which could breach sterility. If the packaging is not properly sealed, the solution might become contaminated, leading to infection risks for patients during medical procedures.
Healthcare workers using Labor Triage Kits for patient care are most at risk, particularly those handling the kits in clinical settings where sterility is critical.
Check for the Labor Triage Kit label with reference code DYKM1564 and lot numbers 24EBR566. The kits are sold with UDI/DI numbers 10889942754571 (each unit) and 40889942754572 (case).
Look for the label 'LABOR TRIAGE KIT, REF DYKM1564' and lot number 24EBR566 on the packaging.
Reach out to Medline directly for assistance with the recall process or to confirm if your kit is affected.
The BD ChloraPrep Clear applicators in these kits may have an open seal, which could breach sterility and lead to infection risks for patients.
Check for the label 'LABOR TRIAGE KIT, REF DYKM1564' and lot number 24EBR566 on the packaging.
Contact Medline directly for assistance with the recall process or to confirm if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2153-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-2153-2025 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.
