Medline recalls surgical convenience kits with perforated sterile bags that risk contamination. Only inner contents stay sterile; affected kits have reorder number DYNDA2489.
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 plastic bag has a perforation that prevents the outside from staying sterile. This means only the contents inside the bag remain sterile, increasing infection risk during procedures.
The plastic bag has a perforation that allows contaminants to reach the outside of the kit. This means the sterile wrapping isn't fully protective, so only the items inside the bag stay sterile. If the bag isn't sealed properly, infection risks increase during medical procedures.
Healthcare professionals using these kits for surgeries or procedures are most at risk. Patients receiving care with these kits could face infection if the sterile field is compromised.
Check for kits labeled 'MEDLINE PLASTICS/PEDS KIT' with reorder number DYNDA2489. The product has a GTIN 41093489695366 and lot number 22BMH128.
Look for the label 'MEDLINE PLASTICS/PEDS KIT' with reorder number DYNDA2489.
The plastic bag has a perforation that prevents the outside from staying sterile, so only the contents inside the bag remain sterile.
Check for kits labeled 'MEDLINE PLASTICS/PEDS KIT' with reorder number DYNDA2489, GTIN 41093489695366, and lot number 22BMH128.
The recall record doesn't 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-1116-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1116-2023 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.
