Medline recalls sterile procedural trays labeled 'Ambulatory Mini Pack' due to potential blade puncture through foil packaging. Affected units include specific lot numbers and item codes.
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 'Ambulatory Mini Pack' because sterile blades inside the trays could puncture the outer foil packaging. This risk could lead to contamination of the trays and compromise medical procedures.
Sterile blades inside the trays may puncture the outer foil layer of the packaging. This could allow contamination of the trays, potentially leading to infections during medical procedures.
Healthcare professionals using these trays for medical procedures are most at risk. Patients receiving procedures using recalled trays could face contamination.
Check for the label 'Ambulatory Mini Pack' on the tray. Affected units have specific lot numbers (22HBQ045) and item codes (DYNJ82579).
Look for the label 'Ambulatory Mini Pack' on the tray.
Sterile blades inside the trays could puncture the outer foil packaging, risking contamination during medical procedures.
Check for the label 'Ambulatory Mini Pack' on the tray. If you have it, contact Medline for instructions.
The recall is due to potential contamination risk, not direct injury. The hazard does not involve physical harm like cuts or fires.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1087-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1087-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
