medical MODERATE Updated 2018-02-28

Covidien LLC recalls Endo GIA Auto Suture Universal Articulating Loading Unit for

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Recalled Product

Endo GIA Auto Suture Universal Articulating Loading Unit for use in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.

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Hazard / Issue

Potential for failure of the device safety interlock. The safety interlock prevents an empty single-use loading unit from being fired a second time.

Issued by

FDA

Distribution: Nationally
Lot/Code Info: N7F1058KX, N7F1121KX, N7F1056KX, N7F1057KX

✅ 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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