Medline recalls CABG surgical kits with perforated sterile bags that risk contamination. Only inner kit contents are sterile; affected kits have reorder number DYNDA282:27.
The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.
Medline is recalling surgical convenience kits labeled as CABG PACK with a specific reorder number because the sterile bag has a perforation. This means only the contents inside the bag are sterile, and the outside wrapping may become contaminated. If you have this kit, stop using it to avoid potential infection risks.
The sterile bag has a perforation that allows non-sterile materials to come into contact with the kit's contents. This means the outside wrapping of the bag is no longer sterile, potentially contaminating the surgical instruments inside. As a result, the risk of infection increases during procedures.
Surgical professionals and hospitals using Medline CABG surgical kits with reorder number DYNDA2827 are most at risk. Patients undergoing surgery with these kits could face contamination risks.
Check for surgical kits labeled 'MEDLINE CABG PACK' with reorder number DYNDA2827. The kit also has a GTIN 401934899531530 and lot number 22HMH432.
Look for the label 'MEDLINE CABG PACK' with reorder number DYNDA2827 on the kit.
The sterile bag has a perforation that allows non-sterile materials to contact the kit's contents, meaning only the inner items are sterile.
Check for the label 'MEDLINE CABG PACK' with reorder number DYNDA2827, GTIN 401934899531530, or lot number 22HMH432.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1112-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1112-2023 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.
