Medline recalls surgical convenience kits with perforated sterile bags that risk contamination. Only inner kit contents remain sterile. Affected kits have specific labels and reorder numbers.
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 because the sterile bag has a perforation that allows non-sterile material to touch the kit's contents. This means only the items inside the bag are sterile, increasing infection risk during procedures.
The surgical kit's outer bag has a perforation that breaks the sterile barrier. This allows non-sterile materials to contact the kit's contents, meaning only the items inside the bag remain sterile. The risk is primarily for procedures requiring strict sterile conditions.
Healthcare professionals using these kits for surgeries or procedures are most at risk. Patients receiving procedures with these kits could face infection if the sterile contents are compromised.
Check for kits labeled 'CENTURION MEDICAL PRODUCTS L & D TRAY' with reorder number MNS9065. The kit also has GTIN 40653160274385 and lot number 22HMF916.
Look for the label 'CENTURION MEDICAL PRODUCTS L & D TRAY' with reorder number MNS9065.
The sterile bag has a perforation that allows non-sterile materials to contact the kit's contents, meaning only the items inside the bag remain sterile.
The recall record does not specify a remedy or action steps beyond checking the label.
Yes, it risks infection during procedures because the sterile barrier is compromised.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1117-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1117-2023 from Medline Industries. 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.
