MEDLINE recalls ReNewal Ligasure Blunt Tip Sealer devices with incomplete packaging seals that could lead to improper use during surgery. Affected units include specific lot numbers and model REF LF1844CR.
Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
MEDLINE is recalling ReNewal Ligasure Blunt Tip Sealer/Divider devices that may have incomplete packaging seals. This could lead to improper use during surgical procedures if the seal is not properly closed.
The packaging seal may not be properly closed, which could lead to improper use of the device during surgery. This might cause the device to malfunction or not function as intended in critical medical procedures.
Surgical professionals who use the ReNewal Ligasure Blunt Tip Sealer/Divider devices are likely affected. Patients undergoing surgery with these devices may be at risk if the packaging seal is incomplete.
Check for the model REF LF1844CR and lot numbers 498004 on the packaging. The device is sold as an electrosurgical instrument compatible with FT10 generators.
Inspect the packaging for a properly sealed tray to ensure the device is safe for use.
The model number is REF LF1844CR.
Lot number 498004 is affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-0117-2024 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-0117-2024 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.
