Medline recalls IV Team PICC kits with specific lot numbers due to potential non-sterile product if the breather pouch seal is opened. Affected kits may require replacement to prevent infection risks during medical procedures.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling certain IV Team PICC kits because the breather pouch seal might be opened, risking non-sterile product use. This could lead to infections if the kit is used incorrectly during medical procedures.
The breather pouch seal on these kits may open unintentionally, allowing non-sterile product to be used. This could happen if the pouch is opened during handling or storage, increasing infection risk during medical procedures.
Healthcare professionals using the Medline IV Team PICC kits with lot number 23LBS908 are most at risk. Patients receiving procedures with these kits could face infection risks if non-sterile materials are used.
Check for lot number 23LBS908 on the Medline IV Team PICC kit packaging. The product is a medical procedure convenience kit with reference number DYNJ48222.
Inspect the breather pouch seal for any signs of being opened or unsealed.
If the seal is open or unsealed, replace the kit with a new one from the manufacturer.
The affected lot number is 23LBS908.
Look for the lot number 23LBS908 on the packaging. The breather pouch seal may be opened if it's not intact.
No, but if the pouch seal is open or unsealed, you should replace it immediately to prevent infection risks.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0168-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0168-2025 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.
