Medline recalls specific versions of its ReNewal Reprocessed Covidien LigaSure Impact devices due to potential incomplete packaging seals. Affected units include certain lot numbers and model versions. Consumers should check their item numbers and lot numbers for recall details.
Potential for an incomplete seal on the packaging tray.
Medline is recalling specific versions of its ReNewal Reprocessed Covidien LigaSure Impact devices because the packaging may not seal properly. This could lead to contamination or improper use of the medical device if the seal is incomplete.
The packaging tray may not seal completely, potentially allowing contamination or improper use of the medical device. This could lead to issues with the device's sterility or functionality during medical procedures.
Healthcare professionals using Medline's ReNewal Reprocessed Covidien LigaSure Impact devices in medical settings are most at risk. Patients using these devices may also be affected if the packaging seal fails.
Check for item numbers LF4418CR, lot numbers listed (500376, 500379, 500380, etc.), and version numbers 4.0.1.15 or lower. The UDI/DI codes are 20888277680446 (case) or 10888277680449 (each).
Look for item numbers LF4418CR on the packaging or device.
Check if your device has a lot number from the list: 500376, 500379, 500380, 500381, 500382, 500504, 500506, 500548, 500559, 500652, 500695, 500874, 503004, 503289.
The recalled device is Medline ReNewal Reprocessed Covidien LigaSure Impact, Sealer/Divider, Nano-Coated, Compatible w/ FT10 18cm FT10 SW, version 4.0.1.15 or lower.
Check for item numbers LF4418CR and lot numbers listed in the recall notice: 500376, 500379, 500380, 500381, 500382, 500504, 500506, 500548, 500559, 500652, 500695, 500874, 503004, 503289.
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-3094-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-3094-2024 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.
