Recall
FDAHealthSeptember 11, 2025

Ethicon Endo-Surgery Inc — ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80

⚠️ The devices were shipped unsterilized.

Is this relevant to me?

Geography
Unknown
Source agency
FDA
Category
Health
Published
September 11, 2025

International distribution to the countries of United Arab Emirates.

What's affected?

Product
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80
Lot code
904C12

Additional details

UDI-DI: 10705036030881; Lot Number: 904C12

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 3 units.

View original FDA notice →

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