Medline recalls specific medical procedure convenience kits that may allow non-sterile product use if breather pouch seals are opened. Affected kits include radioology trays and cardiac catheter packs with certain lot numbers.
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 specific medical procedure convenience kits that could allow non-sterile products to be used if the breather pouch seal is opened. This poses a risk of infection during medical procedures if the kits are used without proper sterility.
The breather pouch seal on these kits may open or become unsealed, allowing non-sterile products to be used. This could lead to infections during medical procedures if the kits are not properly sealed and handled.
Healthcare professionals and medical facilities that use these kits for procedures like radiology or cardiac catheterization are most at risk. Patients undergoing procedures with these kits could face infection if the seal is compromised.
Check for the product names listed: Radioology LP Tray (REF DYNDH1609), Cardiac Cath Pack-LF (REF DYNJ19010I), and other kits with specific lot numbers like 23LBO852, 23LBK443, etc.
Inspect the breather pouch seal for any signs of being opened or unsealed.
If the seal is open, discard the kit immediately to prevent potential infection.
Affected kits include Radioology LP Tray (REF DYNDH1609), Cardiac Cath Pack-LF (REF DYNJ19010I), and other specific medical procedure convenience kits with lot numbers like 23LBO852, 23LBK443, etc.
Check for the breather pouch seal being opened or unsealed; if visible, the kit is affected.
Discard the kit immediately to prevent potential infection from non-sterile products.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0155-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0155-2025 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.
