Medline recalls specific medical convenience kits containing BD ChloraPrep Triple Swabsticks with potential open seals. Affected kits include Cancer Service Port Kit (SKU DT22710) and Line Kit (SKU DYNDA1857A) with listed lot numbers. Stop using immediately to avoid contamination risks.
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Medline is recalling specific medical convenience kits that contain BD ChloraPrep Triple Swabsticks with a potential open seal in the packaging. This could lead to contamination if the swabsticks are used without the seal intact.
The packaging of the BD ChloraPrep Triple Swabsticks may have an open seal, which could allow contamination. If the seal is compromised, the swabsticks might not be sterile when used, increasing the risk of infection.
Healthcare professionals using the recalled Medline medical kits, particularly those in cancer care or line management. Patients receiving treatments with these kits may be at risk if the swabsticks are contaminated.
Check for the specific kits listed: Cancer Service Port Kit (SKU DT22710) or Line Kit (SKU DYNDA1857A) with lot numbers 25EBC812 or 25FBH991 respectively. These kits were sold with the specified lot numbers between 2023 and 2024.
Discontinue use of the recalled kits containing BD ChloraPrep Triple Swabsticks with open seals to prevent potential contamination.
The affected kits include Cancer Service Port Kit (SKU DT22710) and Line Kit (SKU DYNDA1857A) with lot numbers 25EBC812 and 25FBH991 respectively.
Stop using the kits immediately to avoid potential contamination risks from the open seals.
The recall does not mention a replacement or repair option; affected kits should be discarded.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1329-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1329-2026 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.
