Class II

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

Ethicon Endo-Surgery Inc · September 11, 2025

Reason for Recall

The devices were shipped unsterilized.

Distribution

International distribution to the countries of United Arab Emirates.

Quantity Affected

3 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0147-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.