Medline recalls specific Open Heart kits due to check valve components potentially getting stuck, which could cause improper fluid flow during medical procedures.
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Medline is recalling several Open Heart kits that contain B. Braun IV Administration Sets and Pump Administration Sets. The check valve components might get stuck, potentially causing improper fluid flow during medical procedures.
The check valve in these kits may become stuck in either the open or closed position. This could lead to improper fluid flow during medical procedures, potentially causing treatment complications.
Healthcare professionals using these specific Open Heart kits for cardiac procedures are most at risk. Patients receiving treatments with these kits could experience improper fluid flow if the check valve gets stuck.
Check for kits labeled 'OPEN HEART' with specific SKUs listed in the recall notice. These include items like CDS984289O, DYNJ902879T, and others with lot numbers starting with 25GBY, 25HBI, etc.
Look for 'OPEN HEART' labels on the kits with specific SKUs listed in the recall notice.
The recall is due to customer complaints that the check valve components may become stuck in the open or closed positions, which could cause improper fluid flow during medical procedures.
Affected kits include those labeled 'OPEN HEART' with SKUs such as CDS984289O, DYNJ902879T, DYKM1025D, and others with lot numbers starting with 25GBY, 25HBI, etc.
No immediate stop is required; the recall is for replacement or correction, not an urgent stop. Check the labels and follow the provided steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1050-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1050-2026 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.
