Medline recalls certain RenewalLigasure Blunt Tip Sealers due to potential residual material trapping, which may dislodge rarely. 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 models of their RenewalLigasure Blunt Tip Sealer/Divider devices because certain areas can trap residual material that might become dislodged in rare cases. This could pose a minor risk to users during medical procedures.
The device has areas that can trap residual material, which may remain inside and become dislodged in rare cases. This could potentially cause a minor issue during medical procedures but is not a common or severe hazard.
Healthcare professionals using the specific Medline RenewalLigasure Blunt Tip Sealer/Divider models with the 4.0.1.15 or lower software version are most at risk. The recall affects reprocessed units sold with specific lot numbers.
Check for the model name 'RenewalLigasure Blunt Tip Sealer/Divider', version 4.0.1.15 or lower, and lot numbers 10888277680371 or 20888277680378. The product is reprocessed and sold as electrosurgical accessories.
Verify the model version and lot numbers to confirm if your device is affected.
The product is safe for use in most cases, but Medline recommends checking if your device is affected by this recall due to potential residual material trapping in rare cases.
Medline does not provide a specific remedy for this recall, so check the product details to see if it's affected.
Look for the model name 'RenewalLigasure Blunt Tip Sealer/Divider', version 4.0.1.15 or lower, and lot numbers 10888277680371 or 20888277680378.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0472-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0472-2026 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.
