Medline recalls specific kits containing BD ChloraPrep Triple Swabsticks that may have open packaging, potentially exposing users to contamination. Affected kits include Universal Kit SKU DT22010B and VAD Access Kit SKUs DT22790C.
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 certain kits that contain BD ChloraPrep Triple Swabsticks, which may have an open seal on the packaging. This could lead to contamination if the swabsticks are used without proper protection.
The packaging of the BD ChloraPrep Triple Swabsticks may have an open seal, which could allow contamination if the swabsticks are used without proper protection. This is a packaging issue rather than a direct hazard to the user.
Healthcare professionals and patients using the recalled kits, particularly those handling the BD ChloraPrep Triple Swabsticks. The risk is low as the hazard involves packaging integrity but not immediate harm.
Check for the following kits: Universal Kit SKU DT22010B, VAD Access Kit SKUs DT22790C, and other listed kits with specific lot numbers like 25EBC888, 25EBO566, etc.
Look for the kit SKU and lot number on the packaging to confirm if it's affected. Affected kits include Universal Kit SKU DT22010B and VAD Access Kit SKUs DT22790C with specific lot numbers.
The packaging of the BD ChloraPrep Triple Swabsticks may have an open seal, which could lead to contamination if used without proper protection.
Affected kits include Universal Kit SKU DT22010B, VAD Access Kit SKUs DT22790C, and other listed kits with specific lot numbers like 25EBC888, 25EBO566, etc.
No, the recall indicates a low risk of contamination, so users can continue using the kits but should check for open packaging and follow the provided steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1330-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1330-2026 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.
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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.
