Medline recalls certain LigaSure Impact Curved Large Jaw Sealers due to potential trapped residual material that 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 certain LigaSure Impact Curved Large Jaw Sealers that may trap residual material, which could become dislodged in rare cases. This poses a low risk of injury but requires checking your device model and lot numbers.
The device may trap residual material in certain areas, which could become dislodged in rare cases. This poses a low risk of injury but requires careful handling during use.
Medical professionals using the Medline LigaSure Impact Curved Large Jaw Sealer for surgical procedures are most at risk. Affected units include specific model versions and lots.
Check for the model version 4.0.1.15 or lower on the device. Affected units have UDI/DI numbers 10888277680432 (each) or 20888277680439 (case).
Identify the model version number on the device, which should be 4.0.1.15 or lower.
Confirm the UDI/DI numbers match the affected units: 10888277680432 (each) or 20888277680439 (case).
The product is safe for most uses, but affected units may trap residual material that could become dislodged in rare cases.
Affected model versions are 4.0.1.15 or lower.
Check the model version number on the device and verify the UDI/DI numbers: 10888277680432 (each) or 20888277680439 (case).
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0468-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0468-2026 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.
