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Ethicon Endo-Surgery Inc recalls ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product N
Recalled October 22, 2025 · FDA recall Z-0147-2026 · Ethicon Endo-Surgery
Hazard
The devices were shipped unsterilized. · FDA Class II
Units
3 units
Sold at
International distribution to the countries of United Arab Emirates.
Description
The devices were shipped unsterilized.
Product
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80
Manufacturer(s)
Ethicon Endo-Surgery Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →