Medline recalls C-Section sterile procedural trays with potential for blades to puncture outer foil packaging. Affected items include various C-Section and CDS models with specific lot numbers. Stop using immediately to avoid contamination risks.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling sterile procedural trays used in C-section births. The blades inside these trays could puncture the outer foil packaging, potentially causing contamination. This affects specific models with listed lot numbers.
Sterile blades within the trays can puncture the outer foil layer of the packaging. This could lead to contamination of the sterile items, increasing infection risk during medical procedures.
Healthcare professionals and birth attendants who use Medline's C-Section sterile procedural trays. The risk is highest for those handling the recalled items without proper checks.
Check for specific model labels like 'C-SECTION OR 30 CDS', 'C-SECTION CDS', or similar. Look for lot numbers such as 22JBX603, 22JBX483, and other listed numbers in the product description.
Discard or return the recalled trays to prevent contamination risks.
The recall includes specific C-Section sterile procedural trays with labels like 'C-SECTION OR 30 CDS', 'C-SECTION CDS', and other variants listed in the product description.
Check the label on the tray for specific model names and lot numbers such as 22JBX603, 22JBX483, or other numbers listed in the product description.
If your tray does not match the listed models or lot numbers, it is not affected by this recall.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1092-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1092-2023 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.
