ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80
Reported: October 22, 2025 Initiated: September 11, 2025 #Z-0147-2026
Product Description
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.
Details
- Recalling Firm
- Ethicon Endo-Surgery Inc
- Units Affected
- 3 units
- Distribution
- International distribution to the countries of United Arab Emirates.
- Location
- Blue Ash, OH
Frequently Asked Questions
What product was recalled? ▼
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80. Recalled by Ethicon Endo-Surgery Inc. Units affected: 3 units.
Why was this product recalled? ▼
The devices were shipped unsterilized.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 22, 2025. Severity: Moderate. Recall number: Z-0147-2026.
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