LSL Healthcare recalls Central Line Dressing Kit Model 2519CP due to open seals on BD ChloraPrep Triple Swabsticks. Affected kits may have packaging that doesn't seal properly.
BD ChloraPrep Triple Swabsticks, a component within the kits, exhibit an open seal on the packaging of the applicators.
LSL Healthcare is recalling Central Line Dressing Kit Model 2519CP because the BD ChloraPrep Triple Swabsticks inside have an open seal on their packaging. This could allow contaminants to enter the swabsticks, potentially causing infection during medical procedures.
The open seal on the BD ChloraPrep Triple Swabsticks packaging could allow contaminants to enter the swabsticks. This might lead to infection if the swabsticks are used during medical procedures without proper sterility.
Healthcare professionals using the Central Line Dressing Kit Model 2519CP for medical procedures are most at risk. Patients receiving these kits could be affected if the swabsticks are used improperly.
Check for the model number 2519CP on the kit's packaging. The lot code 5G3119 and expiration date 7/31/26 are also listed on the packaging.
Look for the model number 2519CP and lot code 5G3119 on the kit's packaging.
The recall is for a potential contamination risk, but the official notice does not specify a risk of serious injury or death.
Check for the model number 2519CP and lot code 5G3119 on the kit's packaging.
The official notice does not provide specific action steps for affected kits.
We’ve drafted a message you can send LSL Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1219-2026 — LSL Healthcare LSL Healthcare Hello, I own a LSL Healthcare that is covered by recall Z-1219-2026 from LSL Healthcare. 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.
