Medline recalls sterile procedural trays with a risk of blades puncturing packaging. Affected units include specific lot numbers and item codes. Stop using immediately to prevent contamination.
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 could have blades puncturing the outer foil packaging. This risk could lead to contamination if the tray is used without proper sterilization.
Sterile blades inside the trays could puncture the foil packaging during handling. This might cause contamination of the tray, making it unsafe for medical procedures.
Healthcare professionals using Medline's sterile procedural trays with the specific lot numbers and item codes listed. Those handling surgical kits are most at risk.
Check for the item number DYNJ341: DYNJ34129C, case GTIN 40889942382300, and unit GTIN 10889942382309. The lot number 22IBG550 is also associated with this recall.
Discard the sterile procedural tray if you have the affected lot number or item code.
Sterile blades inside the trays could puncture the foil packaging, risking contamination during medical procedures.
Discard the sterile procedural tray immediately if it has the item number DYNJ34129C, case GTIN 40889942382300, or unit GTIN 10889942382309 with lot number 22IBG550.
The recall record does not mention any replacement options.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1062-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1062-2023 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.
