Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Covidien Endo GIA AutoSuture Universal Loading Unit Recalled by Covidien LP Due to Single Use Loading Unit contained two staples loaded...

Date: February 11, 2013
Company: Covidien LP
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Covidien LP directly.

Affected Products

Covidien Endo GIA AutoSuture Universal Loading Unit, 30mm-2.0mm Product Code: 030450 Applications in abdominal, gynecologic, pediatric anti thoracic surgery for resection, transection and creation of anastomosis.

Quantity: 6,751 units

Why Was This Recalled?

Single Use Loading Unit contained two staples loaded in each cartridge pocket and may result in difficulty firing and removing the device from the application site, which may require medical intervention

Where Was This Sold?

Worldwide Distribution -- USA, Asia Pacific, Canada, Europe, and Japan.

About Covidien LP

Covidien LP has 57 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report