Medline recalls specific blood culture kits with BD ChloraPrep Triple Swabsticks that may have an open seal on packaging, risking contamination during use.
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 blood culture kits labeled as 'BLOOD CULTURE KIT NS' with SKU DYNDH2088. The kits contain BD ChloraPrep Triple Swabsticks that may have an open seal, which could lead to contamination if the swabsticks are used improperly.
The swabsticks may have an open seal on the packaging, which could allow contamination during use. This risk is low because the hazard is related to improper handling and not a direct safety hazard like fire or injury.
Healthcare professionals using Medline blood culture kits with specific SKU and lot numbers are most at risk. Patients receiving these kits may also be affected if the swabsticks are contaminated.
Check for Medline blood culture kits labeled 'BLOOD CULTURE KIT NS' with SKU DYNDH2088. Look for lot numbers 25EBU508 or 25EBE330 on the packaging.
Look for lot numbers 25EBU508 or 25EBE330 on the Medline blood culture kit packaging.
Medline blood culture kits labeled 'BLOOD CULTURE KIT NS' with SKU DYNDH2088 and lot numbers 25EBU508 or 25EBE330.
The kits contain BD ChloraPrep Triple Swabsticks that may have an open seal on the packaging, which could lead to contamination if used improperly.
Check the packaging for lot numbers 25EBU508 or 25EBE330. If you have these kits, contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1333-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1333-2026 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.
