Medline Industries recalls sterile procedural trays including BASIN SET-UP PACK and others due to potential blade puncture in packaging. Affected units have specific item numbers and lot numbers. Stop using immediately to prevent injury.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline Industries is recalling a range of sterile procedural trays, including BASIN SET-UP PACK and others, because sterile blades inside the trays could puncture the outer foil packaging. This risk could lead to injury during medical procedures. Affected units have specific item numbers and lot numbers listed in the recall.
Sterile blades within the trays have the potential to puncture the outer foil layer of the sterile packaging. This could cause contamination or injury if the packaging is compromised during medical procedures.
Healthcare professionals and medical facilities that use these sterile procedural trays are most at risk. The recall affects specific models and lots produced by Medline Industries.
Check for specific product names like BASIN SET-UP PACK, LAP CHOLE CDS, MAJOR CDS, or UROLOGY MINOR CDS. Look for item numbers and lot numbers listed in the recall notice.
Discontinue use of all recalled sterile procedural trays to prevent potential puncture of the outer foil packaging and contamination.
The recall includes specific sterile procedural trays such as BASIN SET-UP PACK, LAP CHOLE CDS, MAJOR CDS, and UROLOGY MINOR CDS, among others. Each has a unique item number and lot number.
Check the product name and lot number against the list of affected items provided in the recall notice. Each product has a specific item number and lot number.
Immediately stop using the product and contact Medline Industries for further instructions.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1079-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1079-2023 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.
