Medline recalls certain LigaSure Maryland Jaw Sealers due to potential residual material trapping. This may dislodge in rare cases. Affected units include specific model versions and lots.
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Medline is recalling specific versions of their LigaSure Maryland Jaw Sealers because residual material can trap inside the device and become dislodged in rare cases. This could pose a risk to users, though serious injury is unlikely.
The device has areas where residual material can get stuck. In rare cases, this material might become dislodged, potentially causing issues during use. However, serious injury is not expected to happen frequently.
Surgical professionals using the Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower are most at risk. Patients receiving this device during surgery may also be affected.
Check for the model version 4.0.1.15 or lower on the device label. Affected units were sold with UDI/DI numbers 10888277719392 (each) or 20888277719399 (case).
Look for the model version number on the device label to confirm if it's affected.
The recall states that residual material can trap inside the device and become dislodged in rare cases, but serious injury is not expected to happen frequently.
Check the device label for model version 4.0.1.15 or lower. Affected units have UDI/DI numbers 10888277719392 (each) or 20888277719399 (case).
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0475-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0475-2026 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.
