Medline recalls certain ligasure impact sealers due to rare risk of residual material dislodging. Affected units include specific model versions sold with FT10 generators.
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 models of their Renewal Ligasure Impact Sealer/Divider devices. The recall is due to a rare possibility that residual material could become dislodged inside the device, though serious injury is not expected.
The device has areas where residual material can get trapped. In rare cases, this material might become dislodged, but serious injury is not expected from this issue.
Healthcare professionals using the Medline Renewal Ligasure Impact Sealer/Divider devices with FT10 generators are most likely affected. Patients using these devices during surgery are at minimal risk.
Check for the model name 'Medline Renewal Ligasure Impact Sealer/Divider NanoCoated', version 4.0.1.15 or lower, sold with FT10 generators. The product has a unique identifier (UDI/DI) listed in the recall notice.
Look for the model name, version number, and UDI/DI codes listed in the recall notice to confirm if your device is affected.
No, the recall is for a rare possibility of residual material becoming dislodged, but serious injury is not expected.
Check for the model name 'Medline Renewal Ligasure Impact Sealer/Divider NanoCoated', version 4.0.1.15 or lower, sold with FT10 generators.
The recall does not require immediate action; check your device details to see if it's affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0469-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0469-2026 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.
