Medline recalls certain LigaSure Maryland Jaw Sealers due to potential residual material trapping. This could rarely dislodge, causing injury. 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 certain areas might trap residual material that could rarely become dislodged. This poses a small risk of injury if the material dislodges.
The device has areas that can trap residual material during use. In rare cases, this material might become dislodged and cause injury. The risk is low because it only happens rarely and requires specific conditions.
Surgical professionals using the Medline LigaSure Maryland Jaw Sealer in medical procedures are most at risk. Patients receiving surgery with this device could be affected if the residual material dislodges.
Check for the model name 'LigaSure Maryland Jaw Sealer/Divider NanoCoated' with version 4.0.1.15 or lower. The product was sold with specific lot numbers and case numbers listed in the recall notice.
Review the model version and lot numbers to confirm if your device is affected.
The recall states that the device has a low risk of residual material dislodging in rare cases, so it is generally safe but should be checked for recall status.
The recall does not specify a remedy, so check the product details to see if it is affected and contact Medline for further instructions.
Look for the model name 'LigaSure Maryland Jaw Sealer/Divider NanoCoated' with version 4.0.1.15 or lower, and check the lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0476-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0476-2026 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.
