Medline recalls medical procedure kits with a slight dimensional variation that may cause fitting difficulties. Affected kits have specific model numbers and lot dates.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling medical procedure kits that may have a slight dimensional variation making them harder to fit into outer canisters. This could cause issues during medical procedures but does not pose a serious injury risk.
The kits have a slight dimensional variation that can make them harder to fit into outer canisters. This could lead to fitting difficulties during medical procedures but does not cause injury or damage to the user.
Medical professionals and facilities using the specific Medline procedure kits with model numbers listed in the recall notice. Those most at risk are users who need precise fitting during medical procedures.
Check for the model numbers: KIT CANISTER SUCT W 12FT, REF DYKM2169. The kits were sold with lot numbers 22IBJ207, 22LBP008, 23ABT182, 23BBK494, 23EBN628, 23GBF762, 23IBF429, 23JBH402, 23LBB872.
Look for the model numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
No, the recall does not require stopping use immediately. The kits have a slight dimensional variation that may cause fitting difficulties but does not pose a serious injury risk.
The recall does not specify a remedy, so no action is required beyond checking your product labels.
The kits may have a slight dimensional variation that could cause fitting difficulties during medical procedures, but this does not pose a serious injury risk.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2709-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2709-2024 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.
