Medline recalls certain medical procedure kits due to a slight dimensional variation that may cause increased difficulty fitting into outer canisters. Affected kits include specific models and lot numbers listed in the recall notice.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling specific medical procedure kits that have a slight dimensional variation which might make them harder to fit into their outer canisters. This could lead to improper use during medical procedures.
The kits have a slight dimensional variation that can cause them to be harder to fit into the outer canisters they're designed for. This might lead to improper use during medical procedures, but it does not pose a direct risk of injury or damage.
Healthcare professionals and medical facilities that use the recalled Medline procedure kits are most at risk. The issue affects kits used in surgeries and procedures involving joints, spine, and extremities.
Check the product label for the model codes listed in the recall, such as ARTHROSCOPY (DYNJ909699), BACK CDS (CDS984000C), or other specific procedure types. Also look for the lot numbers provided in the recall notice.
Look for the model codes and lot numbers listed in the recall notice to determine if your kit is affected.
The recall affects specific medical procedure kits with model codes like ARTHROSCOPY (DYNJ909699), BACK CDS (CDS984000C), and others listed in the recall notice. Each kit has unique lot numbers.
Check the product label for the model codes and lot numbers provided in the recall notice. Affected kits include specific models and lot numbers listed in the notice.
If your kit does not match the model codes or lot numbers listed in the recall, it is not affected by this recall and no action is needed.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2714-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2714-2024 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.
