Medline recalls surgical convenience kits with perforated sterile bags that risk contamination. Only inner contents stay 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, meaning only the contents inside the bag remain sterile. This could lead to infections if the kit is used improperly. Affected kits have specific labels and reorder numbers.
The surgical kit's sterile bag has a perforation, so the outside of the bag isn't sterile. This means that if the bag is handled or opened, contaminants could enter the kit, risking infection for the patient or user.
Healthcare professionals using Medline surgical kits for procedures are most at risk. Patients receiving procedures with these kits could face infection if the sterile bag is compromised.
Check for kits labeled 'MEDLINE ANGIO PORT KIT W/HIGH GRADE IN' with reorder number DYNDC2691 or GTIN 40193489343800. Lot numbers starting with 22HMG394 are also affected.
Look for the specific label and reorder number on the kit packaging to confirm if it's affected.
The sterile bag has a perforation, so only the contents inside the bag remain sterile. This could lead to contamination if the bag is handled improperly.
Check for kits labeled 'MEDLINE ANGIO PORT KIT W/HIGH GRADE IN' with reorder number DYNDC2691 or GTIN 40193489343800 and lot numbers starting with 22HMG394.
The recall doesn't specify a remedy, so contact Medline directly to confirm if your kit is affected and get guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1110-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1110-2023 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.
