Medline recalls specific Heart Overhead Table Packs due to incorrect labeling during manufacturing, potentially causing confusion with different model numbers.
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Medline is recalling certain Heart Overhead Table Packs that were incorrectly labeled as model 30000 instead of 30001 during manufacturing. This labeling error could lead to using the wrong model, which might cause improper use or compatibility issues with medical equipment.
During manufacturing, the recalled table packs were incorrectly labeled as model 30000 instead of model 30001. This labeling error could lead to using the wrong model number, potentially causing improper equipment compatibility or function in medical settings.
Healthcare professionals using Medline Heart Overhead Table Packs with specific lot numbers (24BMD381, 24BMJ452) are affected. Those using the recalled model may face compatibility issues if the wrong model is installed.
Check for the lot numbers 24BMD381 or 24BMJ452 on the table pack. The product is identified by the reference number DYNJ0778508J and UDI/DI codes 40195327563784 (case) or 10195327563783 (each).
Look for lot numbers 24BMD381 or 24BMJ452 on the table pack to confirm if it is recalled.
The table packs were incorrectly labeled as model 30000 instead of model 30001.
Lot numbers 24BMD381 and 24BMJ452 are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0120-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0120-2025 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.
