Medline recalls sterile procedural trays labeled as EP LAB PACEMAKER PACK and other variants due to potential blade puncture in packaging. Affected units include specific lot numbers and item codes. Consumers should stop using these trays immediately.
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 with labels like EP LAB PACEMAKER PACK and OPEN HEART CDS. The trays have a risk of sterile blades puncturing the outer foil packaging, which could lead to contamination. This is a safety issue that requires immediate action.
Sterile blades inside the trays can puncture the outer foil layer of the packaging during use. This could lead to contamination of the blades and the surrounding area, increasing the risk of infection or improper sterilization.
Healthcare professionals and medical facilities that use these specific sterile procedural trays for surgeries or procedures. The risk is highest for those handling the trays without proper safeguards.
Check for trays labeled with specific names like EP LAB PACEMAKER PACK, OPEN HEART CDS, or similar variants. Look for the lot numbers and item codes listed in the recall notice, which include specific dates and identifiers.
Immediately stop using all recalled sterile procedural trays to prevent potential contamination and infection risks.
Trays labeled as EP LAB PACEMAKER PACK, OPEN HEART CDS, PACEMAKER CDS, HEART CDS, and other variants with specific lot numbers and item codes listed in the recall notice.
Check the label on the tray for specific names like EP LAB PACEMAKER PACK or OPEN HEART CDS. Compare the lot number and item code to the list provided in the recall notice.
The recall does not specify a return process, but you should stop using the affected trays immediately to prevent contamination risks.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1067-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1067-2023 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.
