Z-0117-2024Class II

MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR...

Name: Z-0117-2024 MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR...
Creator: MEDLINE INDUSTRIES, LP - Northfield
Published: 2023-08-03
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2023-08-03 / Open, Classified / root cause: packaging

FDA source

MEDLINE INDUSTRIES, LP - Northfield began a recall of MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR. electrosurgical instrument on 2023-08-03. FDA classified it as Class II and gives the reason as "Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0117-2024
Classification: Class II
Status: Open, Classified
Initiated: 2023-08-03
Posted: 2023-10-16
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: MEDLINE ReNewal Ligasure Blunt Tip Sealer/Divider Nano-Coated Compatible with FT10 Generator, REF LF1844CR. electrosurgical instrument
Product code: NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Reason for recall: Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.
Root cause tag: packaging
FDA root cause: Packaging
Action: Medline issued a recall notice to its consignees by email on 08/03/2023. The notice explained the problem and the potential risk. Those consignees who have transferred possession of the affected product were directed to notify their customers. The firm is seeking the return of the affected product. An error in the model number was noted (missing an "R" at the end) and the firm issued an updated letter on 09/19/2023 with the corrected number.
Quantity in commerce: 11 units
Distribution: US
Product codes and lots: UDI/DI 10888277680418 (each), 20888277680415 (case), Lot Numbers: 498004

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0117-2024
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0117-2024	Class II	Ongoing	Voluntary: Firm initiated	2023-10-25	2023-10-16
Z-0118-2024	Class II	Ongoing	Voluntary: Firm initiated	2023-10-25	2023-10-16
Z-0119-2024	Class II	Ongoing	Voluntary: Firm initiated	2023-10-25	2023-10-16
Z-0120-2024	Class II	Ongoing	Voluntary: Firm initiated	2023-10-25	2023-10-16

Product code NUJ

K160333Class IIMedline ReNewal Reprocessed LigaSure Blunt Tip Open Sealer/DividerSurgical Instrument Service and Savings, Inc. / cleared 2016-07-20

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)