Medline recalls sterile procedural trays where blades may puncture foil packaging. Affected items have specific lot numbers and item codes. Consumers should check their packaging for 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 sterile procedural trays that could have blades puncturing the outer foil packaging. This risk might lead to contamination during medical procedures if the packaging is compromised.
Sterile blades inside the trays might puncture the foil packaging during handling or storage. This could allow contaminants to enter the sterile tray, potentially causing infections during medical procedures.
Healthcare professionals using Medline's Universal Core Dr Runnels Pack Sterile Procedural Trays with specific lot numbers and item codes are most at risk. Patients receiving procedures using these trays could also be affected.
Check the tray's packaging for the lot number 22IBJ862, item number DYNJ52230, or unit code 10889942252268. The case UDI/GTIN is 40889942252269.
Look for the lot number 22IBJ862, item number DYNJ52230, or unit code 10889942252268 on the tray's packaging.
The recall is for potential contamination risk if the foil packaging is punctured by the blade, but it is not a direct safety hazard for users.
Check the tray's packaging for the lot number 22IBJ862, item number DYNJ52230, or unit code 10889942252268.
The recall does not specify a remedy, so check the packaging details to determine if your tray is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1064-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1064-2023 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.
