FDAClass IIOctober 25, 2023

MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider recall

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

Why was MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
MEDLINE ReNewal Ligasure Maryland Jaw Sealer/Divider Nano-Coated Complatible with FT10 Generator, REF LF1944CR. electrosurgical instrument
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Quantity
58 units
Distribution
US
Recall date
October 25, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls