medical MODERATE Updated 2025-10-22

Ethicon Endo-Surgery Inc recalls ECHELON LINEAR Cutters Reload 80 mm Blue, intended for trans

See all recalls from Ethicon Endo-Surgery Inc →

Recalled Product

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

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Hazard / Issue

The devices were shipped unsterilized.

Issued by

FDA

Distribution: International distribution to the countries of United Arab Emirates.
Lot/Code Info: UDI-DI: 10705036030881; Lot Number: 904C12

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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