Medline Industries, LP: Medical Device Recall in 2025 - (Recall #: Z-0476-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Product Classification:

Class II

Date Initiated: October 1, 2025

Date Posted: November 19, 2025

Recall Number: Z-0476-2026

Event ID: 97822

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 57,244 units

Code Information:

UDI/DI 10888277719415 (each), 20888277719412 (case), All Lots

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated