Medline recalls anesthesia room kits with specific lot numbers due to potential non-sterile product if breather pouch seal is opened. Affected kits may pose 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 anesthesia room kits that could allow non-sterile products if the breather pouch seal is opened. This poses a risk of infection during medical procedures if the kit is used improperly.
The breather pouch seal may open unintentionally, allowing non-sterile products to enter the kit. This could lead to infections during medical procedures if the kit is used without proper sterility checks.
Healthcare professionals using Medline anesthesia room kits with lot number 23KBQ236 are most at risk. Patients undergoing procedures with these kits could face infection risks if non-sterile products are used.
Check for lot number 23KBQ236 on the breather pouch. The product is a Medline CV Anesthesia Room Setup kit with reference number DYNJ905503F.
Inspect the breather pouch seal for any signs of being opened or unsealed.
The recall affects kits with lot number 23KBQ236. If you have this lot number, there is a risk of non-sterile product if the pouch seal is opened during use.
Look for lot number 23KBQ236 on the breather pouch. The product is a Medline CV Anesthesia Room Setup kit with reference number DYNJ905503F.
If the pouch seal is opened, do not use the kit and contact Medline for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0152-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0152-2025 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.
