Medline recalls sterile procedural trays labeled 'General Endoscopy' due to potential blade puncture of 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 for general endoscopy because the blades inside could puncture the outer foil packaging. This risk could lead to contamination of the trays if the foil is compromised during use.
Sterile blades inside the trays can puncture the outer foil layer of the packaging. If the foil is punctured, the trays may become contaminated, increasing the risk of infection during medical procedures.
Healthcare professionals using these trays for endoscopic procedures are most at risk. Patients and staff handling the trays could be affected if the foil packaging is punctured.
Check for trays labeled 'General Endoscopy' with item number DYNJ903826D. Look for lot number 22IBR004 or unit UDI/GTIN 10195327177799.
Look for the item number DYNJ903826D and lot number 22IBR004 on the tray packaging.
Sterile blades inside the trays can puncture the outer foil layer of the packaging, potentially leading to contamination.
Check for trays labeled 'General Endoscopy' with item number DYNJ903826D and lot number 22IBR004.
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-1075-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1075-2023 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.
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.
