CLASS II ONGOING Device recall · Reported 25 Oct 2023 · FDA Enforcement Report

Medline ReNewal Ligasure Maryland Jaw Sealer/Divider recalled

Medline Industries LP - Northfield is recalling Medline ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10. The recall was initiated on 3 Aug 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI/DI 10888277719439 (each), 20888277719436 (case), Lot Numbers: 498006, 498837, 498838, 499150, 499151

Quantity recalled58 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0118-2024
FDA event ID: 92920
Recalling firm: Medline Industries LP - Northfield, Northfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 3 Aug 2023
FDA classified: 16 Oct 2023
Reported: 25 Oct 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Packaging Defects
Device type: Surgical Instruments

Timeline

3 Aug 2023	Recall initiated by company
16 Oct 2023	Classified by FDA	+74 days
25 Oct 2023	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. electrosurgical instrument

Where it was distributed

Questions about this recall

Why was it recalled?

Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

Which lots are affected?

UDI/DI 10888277719439 (each), 20888277719436 (case), Lot Numbers: 498006, 498837, 498838, 499150, 499151

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 92920

This product is part of a recall event; the main page for the event is Medline ReNewal Harmonic ACE+7 Shears w/ Adv recalled.

Reported	Class	Recall	Company	Reason	Where
25 Oct 2023	CLASS II	Medline ReNewal Harmonic ACE+7 Shears w/ Adv recalled	Medline Industries LP - Northfield	Packaging Defects	IL
25 Oct 2023	CLASS II	Medline ReNewal Ligasure Sealer/Divider Nano-Coated recalled	Medline Industries LP - Northfield	Packaging Defects	IL
25 Oct 2023	CLASS II	Medline ReNewal Ligasure Blunt Tip Sealer/Divider recalled	Medline Industries LP - Northfield	Packaging Defects	IL

More recalls from Medline Industries LP - Northfield

All 792

Reported	Class	Recall	Company	Reason	Where
1 Oct 2025Device	CLASS I	Medline medical convenience kits labeled as recalled	Medline Industries LP - Northfield	Device Malfunction	6 states
1 Oct 2025Device	CLASS I	Medline medical convenience kits labeled as recalled	Medline Industries LP - Northfield	Device Malfunction	6 states
3 Sep 2025Device	CLASS I	Medline ReNewal Reprocessed St. Jude Medical Response recalled	Medline Industries LP - Northfield	Particulate Matter	Nationwide
3 Sep 2025Device	CLASS II	The Medline General Surgery Tray is customized to meet recalled	Medline Industries LP - Northfield	Sterility	Nationwide
3 Sep 2025Device	CLASS II	Medline Kits containing BD SureStep Foley Tray Systems recalled	Medline Industries LP - Northfield	Labeling Errors	FL, IL

Other Surgical Instruments recalls

All 3,809

Reported	Class	Recall	Company	Reason	Where
9 Sep 2026Device	CLASS II	Medline Convenience Kits: IV Start KIT recalled by Medline Industries	Medline Industries	Sterility	Nationwide
9 Sep 2026Device	CLASS II	Medline Convenience Kits containing BD ChloraPrep Clear recalled	Medline Industries	Packaging Defects	Nationwide
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: Open Heart Pack, Medline Kit recalled	Medline Industries	Other	Nationwide
2 Sep 2026Device	CLASS II	Medline convenience kits labeled as: GYN Robotic CDS, Medline Kit recalled	Medline Industries	Other	Nationwide
2 Sep 2026Device	CLASS II	Linvatec Genesys CrossFT Suture Anchor with Disposable Driver recalled	ConMed	Other	Nationwide