Medline recalls 16 different GYN robotic surgical kits with potentially contaminated components. Consumers should stop using these kits immediately to avoid health risks.
Kits contain a potentially contaminated component which were recalled by the manufacturer
Medline is recalling 16 specific surgical kits used in gynecological robotic procedures because they contain a potentially contaminated component. Using these kits could pose a health risk to patients and medical staff.
The kits contain a component that was found to be potentially contaminated by the manufacturer. This contamination could lead to health risks if the kits are used in medical procedures without proper cleaning or sterilization.
Medical professionals and patients who use these specific Medline surgical kits for gynecological robotic procedures are affected. Those who have the kits listed in the recall are at risk of exposure to contamination.
Check the kit's label for the product name and SKU code. The recalled kits include items like 'GYN ROBOTIC CDS' (SKU CDS982888Q) and 'GYN ROBOTIC ADD ON PACK' (SKU DYNJ43837D). Each kit has a specific lot number and UDI/DI code listed in the recall.
Immediately stop using any recalled Medline surgical kits to avoid potential health risks from contaminated components.
Medline recalls 16 different surgical kits including GYN ROBOTIC CDS (SKU CDS982888Q), GYN ROBOTIC ADD ON PACK (SKU DYNJ43837D), and others with specific lot numbers and UDI/DI codes listed in the recall.
Check the kit's label for the product name and SKU code. The recalled kits have specific lot numbers and UDI/DI codes listed in the recall notice.
Immediately stop using the kit and contact Medline directly for further instructions on disposal or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3025-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-3025-2026 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.
