Ethicon Endo-Surgery Inc: Medical Device Recall in 2025 - (Recall #: Z-0147-2026)

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:

ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80

Product Classification:

Class II

Date Initiated: September 11, 2025

Date Posted: October 22, 2025

Recall Number: Z-0147-2026

Event ID: 97654

Reason for Recall:

The devices were shipped unsterilized.

Status: Ongoing

Product Quantity: 3 units

Code Information:

UDI-DI: 10705036030881; Lot Number: 904C12

Distribution Pattern:

International distribution to the countries of United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated