Medline recalls Adult Anesthesia Sets with specific lot numbers due to potential leaking Clearlink IV Sets from Baxter. Affected units may cause injury if used improperly.
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
Medline is recalling adult anesthesia sets with lot number 25GMB464 because some kits contain Clearlink IV sets that Baxter previously recalled for leaking. This could lead to injury if the leaking sets are used during medical procedures.
The Clearlink IV sets in some Medline kits were recalled by Baxter due to customer reports of leaking. Leaking IV sets could cause contamination or injury during medical procedures if not properly managed.
Healthcare professionals using Medline Adult Anesthesia Sets with lot number 25GMB464 are most at risk. Patients receiving anesthesia from these sets could be affected if the leaking sets are used.
Check your Medline Adult Anesthesia Set for lot number 25GMB464. The product code is REF DYNJ39985G with UDI/DI numbers 10198459062353 (EA) or 40198459062354 (Case).
Look for lot number 25GMB464 on the Medline Adult Anesthesia Set packaging or label.
Medline recalls these anesthesia sets because some contain Clearlink IV sets that Baxter previously recalled for leaking, which could cause injury during medical procedures.
The recall record does not specify a remedy, so check with Medline directly for instructions.
Affected units have lot number 25GMB464 and product code REF DYNJ39985G with UDI/DI numbers 10198459062353 (EA) or 40198459062354 (Case).
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0137-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0137-2026 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.
