Covidien, LP recalls Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal, gynecologic, pediatric and thoracic surg

Recalled June 5, 2024 · FDA recall Z-1891-2024 · Covidien

Hazard

Potential damage to the cartridge can result in poor staple formation and/or incomplete staple line, may cause a delay in surgery · FDA Class II

Units

1681 units

Sold at

Worldwide - US Nationwide distribution in the state of NJ and the countries of Australia, Japan, New Zealand, Saudi Arabia, Singapore, South Africa, Taiwan, Thailand.

Description

Potential damage to the cartridge can result in poor staple formation and/or incomplete staple line, may cause a delay in surgery

Product

Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection of tissue and creation of anastomosis Model: SIGTRSB60AXT

Manufacturer(s)

Covidien, LP

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →