Covidien, LP: Medical Device Recall in 2024 - (Recall #: Z-1891-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 15, 2024

Date Posted: June 5, 2024

Recall Number: Z-1891-2024

Event ID: 94484

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1681 units

Code Information:

GTIN: 10884521717633 20884521717630 Lot #: N3G1372Y

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated