Medline recalls sterile procedural trays labeled MINOR BASIC PACK-LF due to potential blade puncture of outer 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 MINOR BASIC PACK-LF because sterile blades inside the trays could puncture the outer foil packaging. This risk could lead to contamination of the trays if the foil is compromised.
Sterile blades inside the trays can puncture the outer foil layer of the packaging. This could compromise the sterility of the trays, potentially leading to contamination during medical procedures.
Healthcare professionals using these trays for sterile procedures are most at risk. Patients and staff handling the trays could be affected if the foil packaging is punctured.
Look for trays labeled 'MINOR BASIC PACK-LF' with item number DYNJ0281516M, case UDI/GTIN 40889942056676, and unit UDI/GTIN 10889942056675. Lot numbers 22JMA630 and 22HMC805 are also affected.
Verify the label and item numbers on the tray to confirm it is affected.
Sterile blades inside the trays have the potential to puncture the outer foil layer of the sterile packaging, which could compromise sterility.
Look for trays labeled 'MINOR BASIC PACK-LF' with item number DYNJ0281516M, case UDI/GTIN 40889942056676, and unit UDI/GTIN 10889942056675. Lot numbers 22JMA630 and 22HMC805 are affected.
The recall record does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1084-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1084-2023 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.
