Medline recalls anesthesia circuit kits with slight dimensional variations that could make fitting into outer canisters harder. Affected kits include specific model numbers and lot ranges. No action required but check for fit issues.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling certain anesthesia circuit kits due to a slight dimensional variation that might make them harder to fit into outer canisters. This could cause minor fitting issues during medical procedures but does not pose a serious safety risk.
The kits have a slight dimensional variation that could make them harder to fit into outer canisters. This might cause temporary fitting issues during medical procedures but does not involve a risk of injury or serious harm.
Medical professionals using the recalled anesthesia circuit kits are most at risk. Patients using these kits during procedures may experience temporary fitting difficulties.
Check for model numbers: ANESTHESIA CIRCUIT ADULT (REF DYNJAAF6666B), ANESTHESIA CIRCUIT PEDS-LF (REF DYNJAP9918A), or CV ANESTHESIA - ROOM SET UP (REF DYNJ905503F). Lot numbers include 22EBD700, 22GBK692, 22KBE980, 23DBF522, etc.
Inspect if the kit fits easily into the outer canister; if it's difficult, it may be affected.
No action is required. The recall is for potential fitting issues, not safety risks.
Affected models include ANESTHESIA CIRCUIT ADULT (REF DYNJAAF6666B), ANESTHESIA CIRCUIT PEDS-LF (REF DYNJAP9918A), and CV ANESTHESIA - ROOM SET UP (REF DYNJ905503F).
Check the lot numbers listed in the recall notice: 22EBD700, 22GBK692, 22KBE980, 23DBF522, etc.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2700-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2700-2024 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.
