Medline recalls sterile procedural trays with potential for blades to puncture packaging foil. Affected models include Celebration Robotic CDS and DAVINCI CDS UCC-LF. 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 may have blades puncturing the outer foil packaging. This could lead to contamination during medical procedures. Affected items include specific robotic surgical kits with labeled model numbers.
Sterile blades inside the trays can puncture the foil layer of the packaging. This creates a risk of contamination during surgical procedures, potentially leading to infections or other complications.
Healthcare professionals using Medline's sterile procedural trays for robotic surgery are most at risk. Patients undergoing procedures with these kits could face contamination if the packaging is compromised.
Check for model labels like 'CELEBRATION ROBOTIC CDS', 'DAVINCI CDS UCC-LF', or 'ROBOTICS PACK-LF' on the trays. Look for specific lot numbers such as 22KBE707, 22JBX839, or 22JBX843.
Discard any sterile procedural trays with the listed model numbers and lot numbers to prevent contamination.
Sterile procedural trays labeled as CELEBRATION ROBOTIC CDS, DAVINCI CDS UCC-LF, or ROBOTICS PACK-LF with specific lot numbers like 22KBE707 or 22JBX839.
Look for model labels on the tray and check the lot numbers listed in the recall notice, such as 22KBE707, 22JBX839, or 22JBX843.
Discard the tray immediately to prevent contamination during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1094-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-1094-2023 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.
