Ethicon Endo-Surgery Inc recalls ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product…
- Recall date
- September 11, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0147-2026
- FDA classification
- Class II
- Brand / firm
- Ethicon Endo-Surgery Inc
- Sold / distributed
- International distribution to the countries of United Arab Emirates.
Why it was recalled
The devices were shipped unsterilized.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80
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