Medline recalls specific medical kits with BD ChloraPrep Triple Swabsticks that may have open packaging seals. Affected kits include POWERGLIDE DRESSING CHANGE KIT SKU DYNDH1576 and CENTRAL LINE TRAY W/ CHLRP SWB SKU RWM-DC57KC. Stop using if you have these kits.
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 two specific medical convenience kits that contain BD ChloraPrep Triple Swabsticks with a potential open seal on the packaging. This could lead to contamination or improper use of the swabsticks if the seal is compromised.
The packaging of the BD ChloraPrep Triple Swabsticks may have an open seal, which could allow contamination or improper use of the swabsticks. This poses a risk if the seal is compromised during storage or handling.
Healthcare workers and patients using Medline's POWERGLIDE DRESSING CHANGE KIT (SKU DYNDH1576) or CENTRAL LINE TRAY W/ CHLRP SWB (SKU RWM-DC57KC) from specific lots. Those handling medical supplies are most at risk.
Check for the kit SKU DYNDH1576 with lot number 25EBP737 or SKU RWM-DC57KC with lot number 25EBE082. These kits were sold with specific UDI/DI numbers.
Look for the specific SKU and lot number on the packaging to confirm if your kit is affected.
The BD ChloraPrep Triple Swabsticks in these kits may have an open seal on the packaging, which could lead to contamination or improper use.
The POWERGLIDE DRESSING CHANGE KIT (SKU DYNDH1576) with lot number 25EBP737 and the CENTRAL LINE TRAY W/ CHLRP SWB (SKU RWM-DC57KC) with lot number 25EBE082.
The recall does not require immediate stop use; however, you should check if your kit is affected and take action if it is.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1331-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1331-2026 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.
