Medline recalls sterile procedural trays (Universal Plastic and Knee Arthroscopy Pack) due to potential blade puncture of packaging. Affected units have specific lot numbers and item numbers. Consumers should contact Medline for details.
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 labeled as Universal Plastic and Knee Arthroscopy Pack because sterile blades inside the trays could puncture the outer foil packaging. This risk could lead to contamination of the sterile items during use.
Sterile blades inside the trays could puncture the outer foil layer of the packaging. This might cause contamination of the sterile items, potentially leading to infections during medical procedures.
Healthcare professionals using these trays for surgical procedures are most at risk. Patients receiving procedures using these trays may also be affected if the packaging is compromised.
Check for the Universal Plastic or Knee Arthroscopy Pack labels. Affected units have specific lot numbers: 22IBH860, 22IBJ054 for Universal Plastic and 22JBM001 for Knee Arthroscopy Pack.
Reach out to Medline Industries for specific details about your product and instructions on how to handle affected units.
Sterile blades inside the trays could puncture the outer foil layer of the packaging, potentially causing contamination during medical procedures.
Check for the Universal Plastic or Knee Arthroscopy Pack labels. Affected units have specific lot numbers: 22IBH860, 22IBJ054 for Universal Plastic and 22JBM001 for Knee Arthroscopy Pack.
Contact Medline Industries for specific details about your product and instructions on how to handle affected units.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1080-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1080-2023 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.
