Medline recalls endoscopy procedure kits with slight dimensional variations that may cause fitting issues with outer canisters. Affected kits include specific model numbers and lot dates.
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 could make them harder to fit into outer canisters. This issue doesn't pose a safety risk but might cause operational difficulties during medical procedures.
The kits have a slight dimensional variation that may cause increased difficulty fitting into outer canisters. This could lead to operational challenges during medical procedures but does not involve physical harm or injury.
Medical professionals using Medline endoscopy kits with the specified model numbers and lot dates are most likely affected. Patients using these kits are not directly impacted.
Check for the model number ENDO KIT, REF DYKE1410A or the specific lot numbers listed in the recall notice. The kits were sold with the indicated model and lot dates.
Verify the model number and lot numbers listed in the recall notice to confirm if your kit is affected.
No, this recall addresses a potential operational difficulty during medical procedures, not a safety hazard.
The recall does not specify a remedy, so no action is required unless you experience fitting issues.
Endoscopy kits labeled ENDO KIT, REF DYKE1410A with specific lot numbers: 22EBO806, 22GBW168, 22IBP461, 22LBC090, 22LBM513, 23BBP271, 23DBM055, 23EBQ913, 23GBI842, 23IBF978, 23KBK768.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2706-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2706-2024 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.
