# FDA recall Z-0147-2026

> **Ethicon Endo-Surgery Inc** · Class II · device recall initiated 2025-09-11.

## Product

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

## Reason for recall

The devices were shipped unsterilized.

## Distribution

International distribution to the countries of United Arab Emirates.

## Key facts

- **Recall number:** Z-0147-2026
- **Recalling firm:** Ethicon Endo-Surgery Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-11
- **Report date:** 2025-10-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Blue Ash, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0147-2026

## Citation

> AI Analytics. FDA recall Z-0147-2026. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0147-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*