Medline recalls specific convenience kits containing semi-rigid suction liners made between September 2023 and November 2023 due to potential loss of suction during use. Affected kits include OPEN HEART KIT, ENDO KIT, and others with specific pack numbers.
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 convenience kits with semi-rigid suction liners made from September to November 2023. These liners may lose suction during intermittent use, which could lead to improper medical suctioning.
The suction liners may lose suction during intermittent use, which could lead to improper medical suctioning. This might cause ineffective treatment or complications during medical procedures.
Healthcare professionals using Medline convenience kits with specific suction liners from September to November 2023 are affected. Those handling the recalled kits are most at risk.
Check for specific pack numbers: DYK1002174I, DYKE1558B, DYKE1804A, DYNJ900714C, DYNJ905472B, or DYNJ908096A. The kits were manufactured between September 2023 and November 2023.
Identify the pack number on the kit label to confirm if it's affected.
Reach out to Medline Industries for assistance with returning or replacing the kit.
The affected kits include OPEN HEART KIT (pack number DYK1002174I), ENDO KIT (pack numbers DYKE1558B and DYKE1804A), VASCULAR-LF (pack number DYNJ900714C), MAJOR CARDIOVASC ADULT (pack number DYNJ905472B), and AV FISTULA (pack number DYNJ908096A).
The kits were manufactured between September 2023 and November 2023.
Check the pack number on the kit label. Affected kits have specific pack 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-3107-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3107-2024 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.
