Medline recalls sterile procedural trays with potential for blades to puncture outer foil packaging. Includes GYN-URO LAPSCP CDS-LF and other surgical kits. No remedy specified.
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 used in surgeries that may have blades puncturing the outer foil packaging. This could lead to contamination or injury if the packaging is compromised during use.
Sterile blades inside the trays can potentially puncture the outer foil layer of the packaging. This could compromise the sterility of the tray and lead to contamination if the packaging is breached during surgical procedures.
Surgical staff and hospitals using Medline's sterile procedural trays with the listed model numbers. Patients are not directly at risk as the hazard occurs during handling by medical professionals.
Check for model numbers like GYN-URO LAPSCP CDS-LF, ROBOTIC CDS, or GYN LAPAROSCOPY CDS-LF with specific lot numbers listed in the recall notice.
Review the model numbers and lot numbers listed in the recall notice to confirm if your specific tray is affected.
No, the hazard occurs during handling by medical professionals, not during patient use. Patients are not directly at risk.
The recall does not specify a remedy, so check the model numbers and lot numbers to determine if your tray is affected. If affected, contact Medline for further instructions.
Look for model numbers such as GYN-URO LAPSCP CDS-LF, ROBOTIC CDS, or GYN LAPAROSCOPY CDS-LF with the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1091-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1091-2023 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.
