Medline recalls sterile surgical trays with potential for blades to puncture foil packaging. Check product labels for specific model numbers and lot numbers listed in the recall notice.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling certain sterile surgical trays used in knee and shoulder arthroscopy procedures. The trays contain blades that could puncture the outer foil layer of the packaging, potentially leading to contamination.
Sterile blades inside the trays can puncture the outer foil layer of the packaging. This could lead to contamination of the surgical instruments if the packaging is compromised during use.
Healthcare professionals who use these specific sterile surgical trays for arthroscopic procedures are likely affected. The risk is low as the hazard is related to packaging integrity rather than direct harm to users.
Check for product labels with model numbers like CDS-LF, CDS, or LV. Look for lot numbers such as 22JBR468, 22JBA443, or similar in the list provided in the recall notice.
Look for model numbers and lot numbers listed in the recall notice to identify affected items.
Sterile blades within the trays have the potential to puncture the outer foil layer of the packaging, which could lead to contamination.
Sterile procedural trays labeled as KNEE ARTHROSCOPY CDS-LF, ARTHROSCOPY CDS, ARTHROSCOPY LV, and other specific models with corresponding lot numbers.
Check the product label for the model number and lot number listed in the recall notice.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1097-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1097-2023 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.
