Reported Oct 7, 2020 · Ongoing

Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm, Item Code 030451 - Product Usage: The Endo GIA…

Covidien, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Covidien, LP · 60 Middletown Ave · North Haven, CT · 06473-3908

Is this the product you have?

  • Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm
  • Item Code 030451 - Product UsageThe Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis
Lot codes and dates
  • Lot Numbers

    62 of 62 codes

    • T0A016X
    • T8D009X
    • T8E058X
    • T8H024X
    • T9D052X
    • T0B130X
    • T8D010X
    • T8E069X
    • T8H025X
    • T9D149X
    • T0D070X
    • T8D012X
    • T8H004X
    • T8H061X
    • T9E081X
    • T7H001X
    • T8D013X
    • T8H008X
    • T8M044X
    • T9E082X
    • T7L024X
    • T8D041X
    • T8H009X
    • T9A032X
    • T9F133X
    • T7L025X
    • T8D042X
    • T8H010X
    • T9A033X
    • T9G029X
    • T8B012X
    • T8D043X
    • T8H011X
    • T9A082X
    • T9G037X
    • T8B013X
    • T8D044X
    • T8H012X
    • T9B039X
    • T9G085X
    • T8C026X
    • T8D045X
    • T8H013X
    • T9B040X
    • T9G086X
    • T8C027X
    • T8D046X
    • T8H014X
    • T9D043X
    • T9G093X
    • T8C045X
    • T8E049X
    • T8H022X
    • T9D050X
    • T9K069X
    • T8C046X
    • T8E050X
    • T8H023X
    • T9D051X
    • T9M069X
Amount recalled
900,007 total

This recall covers 9 products

The agency filed one notice per product. You are reading one of them; the other 8 are below.

Where it was sold

  • Nationwide

Why it was recalled

The device staples may not properly form upon application preventing adequate hemostasis. Use of a product with this assembly error may result in incomplete staple formation.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.