Medline recalls specific models of jaw sealers due to potential incomplete packaging seals. Affected units may have packaging issues; contact Medline for details.
Potential for an incomplete seal on the packaging tray.
Medline is recalling certain models of jaw sealers that may have incomplete packaging seals. This could lead to packaging issues during use, though the risk is not severe.
The packaging tray may not seal completely, potentially causing issues with the device during use. However, the hazard is not described as causing serious injury or death.
Healthcare professionals using the Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider may be affected. Those with the specific model numbers listed are most at risk.
Check for the model number LF1937CR on the packaging. Affected units have specific lot numbers listed in the recall notice, including many numbers starting with 514000.
Look for the model number LF1937CR and lot numbers listed in the recall notice.
The recall states there is a potential for an incomplete seal on the packaging tray, but it does not indicate a risk of serious injury or death.
Check the product label for model number LF1937CR and lot numbers from the list provided in the recall notice.
The recall does not specify a remedy, so contact Medline directly for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-3093-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3093-2024 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.
