Medline recalls specific Open Heart 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 Open Heart Packs (model 30001) that were incorrectly labeled as model 30000 during production. This labeling error could lead to using the wrong product in medical procedures, which might cause complications.
During manufacturing, some kits were incorrectly labeled as model 30000 instead of model 30001. This could lead to using the wrong product in medical procedures, potentially causing complications if the wrong model is used.
Healthcare professionals using Medline Open Heart Packs with specific lot numbers (23LBM368, 23LBH354) are affected. Those handling these kits in medical settings are at risk of using the wrong model during procedures.
Check for the specific lot numbers: 23LBM368 or 23LBH354 on the packaging. The product is labeled as 'MEDLINE OPEN HEART PACK, REF DYNJ66216C' with UDI/DI numbers 40193489853361 (case) or 10193489853360 (each).
Look for lot numbers 23LBM368 or 23LBH354 on the packaging.
Medline identified that certain kits were incorrectly labeled as model 30000 instead of model 30001 during manufacturing.
The affected kits are labeled as model 30000 but should be model 30001.
Check for lot numbers 23LBM368 or 23LBH354 on the packaging.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0121-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0121-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
