Medline recalls specific endoscopy kits with 1500 cc semi-rigid suction liners from September to November 2023 due to potential loss of suction during intermittent use. Affected kits include ENDO KIT Pack Numbers DYKE1350D and DYKE1514B.
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
Medline is recalling endoscopy convenience kits with specific suction liners made between September and November 2023. These liners may lose suction or have low suction during intermittent use, which could affect medical procedures.
The recalled suction liners may lose suction or have low suction during intermittent use. This could lead to ineffective removal of fluids or debris during medical procedures, potentially causing complications.
Healthcare professionals using endoscopy kits with the recalled suction liners are most at risk. Patients undergoing procedures with these kits may experience complications due to inadequate suction.
Check for endoscopy kits labeled 'ENDO KIT' with Pack Numbers DYKE1350D or DYKE1514B. The liners were manufactured between September 2023 and November 2023 with specific lot numbers.
Identify the pack number and lot numbers on the suction liners to confirm if they are affected.
Medline is recalling specific endoscopy convenience kits with 1500 cc semi-rigid suction liners made from September to November 2023 due to potential loss of suction during intermittent use.
ENDO KIT kits with Pack Numbers DYKE1350D or DYKE1514B, manufactured between September 2023 and November 2023.
The recall record does not specify a remedy, so check with Medline Industries 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-3112-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3112-2024 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.
