Medline recalls sterile procedural trays (AV SHUNT CDS, ZALE V-P SHUNT CDS, NEURO CDS-LF, MAJOR) due to risk of sterile blades puncturing outer foil packaging.
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 that may have blades that puncture the outer foil packaging. This could lead to contamination of the sterile contents during medical procedures.
Sterile blades inside the trays can puncture the outer foil layer of the packaging, potentially contaminating the sterile contents during medical procedures. This could lead to infections or other complications.
Healthcare professionals using these specific sterile procedural trays for surgeries or procedures. Patients receiving these trays during medical procedures are at risk of contamination.
Check for trays labeled as AV SHUNT CDS, ZALE V-P SHUNT CDS, NEURO CDS-LF, or MAJOR. These trays have specific item numbers and lot numbers listed in the recall notice.
If you have any of the recalled sterile procedural trays, stop using them immediately to prevent potential contamination.
The recall includes sterile procedural trays labeled as AV SHUNT CDS, ZALE V-P SHUNT CDS, NEURO CDS-LF, and MAJOR, among others with specific item numbers and lot numbers.
Check the tray label for specific item numbers and lot numbers listed in the recall notice, such as AV SHUNT CDS with item number CDS983098D and lot number 22IBD957.
Stop using the tray immediately and contact Medline for instructions on disposal or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1088-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1088-2023 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.
