Medline recalls sterile procedural trays with blades that could puncture packaging foil. Check labels for specific model numbers and lot numbers to determine if your item is affected.
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 which can puncture the outer foil layer of the packaging. This could lead to contamination during medical procedures if the packaging is compromised.
Sterile blades inside the trays have the potential to puncture the outer foil layer of the sterile packaging. If the packaging is compromised, it could lead to contamination during medical procedures.
Healthcare professionals using these trays for surgical procedures are most at risk. Patients undergoing surgery with these trays could be exposed to contamination if the packaging is punctured.
Check the product label for the specific model name (e.g., GYN ABD CDS, LAVH PROCEDURE) and lot number. The affected items have specific item numbers and lot numbers listed in the recall notice.
Look for the model name and lot number on the product label to determine if it's affected.
Reach out to Medline for assistance with the recall if you have the product.
Sterile blades within the trays have the potential to puncture the outer foil layer of the sterile packaging, which could lead to contamination during medical procedures.
Check the product label for the model name (e.g., GYN ABD CDS) and lot number. The affected items have specific item numbers and lot numbers listed in the recall notice.
Contact Medline directly for assistance with the recall. There is no stated remedy in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1093-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1093-2023 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.
