Medline recalls certain Renewal Ligasure Maryland Jaw Sealers due to potential residual material trapping, which may dislodge in rare cases. Affected units have specific model numbers and were sold with FT10 Generator.
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 Maryland Jaw Sealers because small amounts of material can get stuck in the device. This could rarely become loose and cause issues during use, though serious harm is unlikely.
The device has areas where residual material can get trapped. In rare cases, this material might become dislodged during use, potentially causing a small issue. However, serious injury or death is not expected.
Surgical professionals using Medline Renewal Ligasure Maryland Jaw Sealers with FT10 Generator 44 cm models. Those with the specific model numbers or lots listed in the recall are most at risk.
Check for the model number 44 cm FT10 SW Version 4.0.1.15 or lower on the device. The product was sold with FT10 Generator and has specific lot numbers listed in the recall.
Look for the model number 44 cm FT10 SW Version 4.0.1.15 or lower on the device.
The recall states that residual material may trap in rare cases and become dislodged, but serious injury or death is not expected. This is a low-risk issue.
Check for the model number 44 cm FT10 SW Version 4.0.1.15 or lower on the device. The product was sold with FT10 Generator and has specific lot numbers listed in the recall.
The recall does not specify a remedy, so no action is required unless you want to check for the model number.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0477-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0477-2026 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.
