Medline recalls endoscopy procedure kits with a slight dimensional variation that may cause fitting difficulties with outer canisters. Affected kits have specific lot numbers and reference codes.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling endoscopy procedure kits that have a slight dimensional variation which might make them harder to fit into outer canisters. This issue doesn't pose a safety risk but could cause operational challenges during medical procedures.
The kits have a slight dimensional variation that may cause increased difficulty fitting into outer canisters during medical procedures. This could lead to operational challenges but does not involve physical injury or safety hazards.
Medical professionals using Medline endoscopy kits with the specific reference codes and lot numbers listed in the recall notice. Patients using these kits are not directly affected.
Check for the reference code ENDO KIT, REF DYK1012268E1 or the specific lot numbers: 22FBU931, 22HBL619, 22JBG192, 22LBH957, 23CBU467, 23FBS319, 23IBT789, 23KMH977.
Review the reference code and lot numbers on the kit to confirm if it is affected.
No, this recall addresses a potential operational difficulty with fitting the kit into outer canisters, not a safety hazard.
Check the reference code and lot numbers to see if your kit is affected; if so, contact Medline for further instructions.
Look for the reference code ENDO KIT, REF DYK1012268E1 or the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2705-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2705-2024 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.
