Medline recalls surgical convenience kits with perforated sterile bags that may compromise sterility. 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 could lead to infections during medical procedures if the kit is used improperly.
The surgical kit's outer bag has a perforation that allows non-sterile materials to come into contact with the kit's contents. This could compromise sterility during medical procedures, potentially leading to infections.
Healthcare professionals using Medline surgical convenience kits labeled as MEDLINE LCPH LAB DRAW KIT with reorder number DYNDH1641A are most at risk. Patients receiving procedures using these kits could also be affected.
Check for kits labeled 'MEDLINE LCPH LAB DRAW KIT' with reorder number DYND:1641A or GTIN 40195327005830. Lot numbers starting with 22HMH339 also indicate affected units.
Look for the label 'MEDLINE LCPH LAB DRAW KIT' with reorder number DYNDH1641A or GTIN 40195327005830.
The recall is due to a perforation in the sterile bag that allows non-sterile materials to contact the kit's contents, potentially compromising sterility during medical procedures.
Check for kits labeled 'MEDLINE LCPH LAB DRAW KIT' with reorder number DYNDH1641A or GTIN 40195327005830, and lot numbers starting with 22HMH339.
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-1121-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1121-2023 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.
