Medline recalls turnover kits with reference DYKC1289F due to potential fit issues with outer canisters. Affected units include specific lot numbers and model details.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling turnover procedure kits with reference DYKC12:89F because a slight size variation might make them harder to fit into outer canisters. This could cause handling difficulties during medical procedures.
A slight dimensional variation in the kit components can make them harder to fit into outer canisters. This may lead to handling difficulties during medical procedures but does not pose a direct safety risk.
Medical professionals using Medline turnover kits with reference DYKC1289F and specific lot numbers are most at risk. The recall affects a limited number of kits sold in the U.S.
Check for the reference number DYKC1289F on the kit. Affected units have lot numbers 23LBF766 and specific UDI/DI codes: 40195327510917 (case) and 10195327510916 (unit).
Verify the reference number DYKC1289F and lot numbers 23LBF766 with UDI/DI codes 40195327510917 (case) and 10195327510916 (unit).
The recall is due to a slight dimensional variation that may cause increased difficulty fitting into outer canisters during medical procedures.
Check the reference number and lot numbers to see if your kit is affected. If it matches, contact Medline for further instructions.
The recall indicates potential handling difficulties but does not mention a risk of injury. This is considered a low-risk issue.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2710-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2710-2024 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.
