Medline recalls certain versions of ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider for possible incomplete packaging seals. Affected units include specific model numbers and lot numbers listed in the recall notice.
Potential for an incomplete seal on the packaging tray.
Medline is recalling specific versions of their ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider due to a potential incomplete seal on the packaging tray. This could lead to improper handling or contamination risks during medical procedures.
The packaging tray may not seal properly, potentially allowing contamination or improper handling of the device during medical procedures. This could lead to infection risks or device malfunction if the seal is incomplete.
Healthcare professionals using Medline's ReNewal Reprocessed Covidien LigaSure Blunt Tip, Sealer/Divider, specifically those with the listed model numbers and lot numbers. Patients using these devices during medical procedures may be at risk if the packaging seal is incomplete.
Check for the model number LF1837CR and lot numbers listed in the recall notice (e.g., 487233, 487315, etc.). The product is a reprocessed version of the Covidien LigaSure Blunt Tip, Sealer/Divider compatible with FT10 37cm FT10 SW.
Verify your product's model number (LF1837CR) and lot numbers against the list provided in the recall notice.
The recall is due to a potential incomplete seal on the packaging tray, which could lead to contamination or improper handling during medical procedures.
Check your product's model number and lot numbers against the list provided in the recall notice. If it matches, contact Medline for further instructions.
The recall notice does not specify a fix or remedy; affected products should be checked against the list and contacted 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-3092-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3092-2024 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.
