Medline recalls certain medical procedure kits due to slight dimensional variations that could cause fitting difficulties with outer canisters. Affected kits include CYSTO, ENDO KIT, and ENDOSCOPY models with specific reference numbers and lot numbers.
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 outer canisters. This could lead to improper use during medical procedures.
The kits have a slight dimensional variation that can cause them to fit poorly into outer canisters. This might lead to improper use during medical procedures, but the risk is not severe enough to cause serious injury.
Healthcare professionals using the recalled Medline medical procedure kits are most at risk. Patients receiving procedures with these kits may be affected if the kits don't fit properly.
Check for the product names CYSTO, ENDO KIT, or ENDOSCOPY with reference numbers listed in the recall. The specific lot numbers and reference codes are provided in the recall details.
Look for the reference numbers and lot numbers listed in the recall to confirm if your kit is affected.
The recalled kits include CYSTO (REF DYNJ905000D), ENDO KIT (REF DYKE1462A), and ENDOSCOPY models with specific reference numbers and lot numbers listed in the recall.
Check the reference number and lot numbers on your kit against the list provided in the recall details.
The recall does not specify a remedy, so you should check the product details to confirm if your kit is affected and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2704-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2704-2024 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.
