Medline recalls surgical convenience kits with perforated sterile bags that may not keep contents sterile. Affected kits have specific reorder numbers and lot codes.
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 wrapping has a perforation that could allow contaminants to enter the kit. This means the instruments inside might not be sterile, posing a risk during medical procedures.
The surgical kits have a perforated bag that doesn't seal properly. This allows non-sterile materials to come into contact with the instruments inside the kit, potentially causing infections during medical procedures.
Healthcare professionals using these kits for surgeries or procedures are most at risk. Patients receiving treatments with these kits could face infection risks.
Check for the product labeled 'CENTURION MEDICAL PRODUCTS IR INSTRUMENT TRAY' with reorder number SUT1067:5 and lot number 22HMG259. These kits were sold with specific GTIN and lot codes.
Look for the reorder number SUT10675 and lot number 22HMG259 on the kit packaging.
The recall is due to perforated bags that don't keep the kit contents sterile, risking contamination during medical procedures.
Check for the product labeled 'CENTURION MEDICAL PRODUCTS IR INSTRUMENT TRAY' with reorder number SUT10675 and lot number 22HMG259.
The official recall notice does not specify a remedy or action steps beyond checking the kit details.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1126-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1126-2023 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.
