FDA Enforcement Class II Ongoing

Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Recall: Z-0477-2026 · Reported November 19, 2025

Enforcement

Recall Number
Z-0477-2026
Event ID
97822
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Medline Industries, LP
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
November 19, 2025
Initiation Date
October 1, 2025
Classification Date
November 7, 2025
Address
3 Lakes Dr, Northfield, IL, 60093-2753, United States

Description

Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Reason

Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.

Code Info

UDI/DI 10888277719439 (each), 20888277719436 (case), All Lots

Distribution

US Nationwide distribution.

Quantity

9,547 units