Medline recalls TRACH PACK sterile procedural trays due to potential blade puncture of foil packaging. Affected units include specific lot numbers and item codes. Consumers should check their product 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 TRACH PACK sterile procedural trays because sterile blades inside the kits could puncture the outer foil packaging. This risk could compromise the sterility of the tray during medical procedures.
Sterile blades inside the trays could puncture the outer foil layer of the packaging. This might allow contamination of the tray during medical procedures, potentially leading to infections.
Healthcare professionals using the TRACH PACK sterile procedural trays are most at risk. Patients receiving procedures with these trays may be affected if the packaging is compromised.
Check for item number DYNJ46518G, case UDI/GTIN 40195327009169, or unit UDI/GTIN 10195327009168. Lot numbers 22JMB321, 22JMA904, and 22HMD287 are also affected.
Verify your TRACH PACK has the item number DYNJ46518G, case UDI/GTIN 40195327009169, or unit UDI/GTIN 10195327009168.
The recall is for potential packaging compromise, but the risk of infection is low if the tray is used properly.
Check for item number DYNJ46518G, case UDI/GTIN 40195327009169, unit UDI/GTIN 10195327009168, or lot numbers 22JMB321, 22JMA904, 22HMD287.
No action is required if your product is not affected. Only check the details to confirm if it's in the recall list.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1061-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1061-2023 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.
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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.
