Recall Z-0004-2021

Covidien, LP · initiated August 12, 2020

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 2.0 mm, Item Code 030453 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.

Codes / lots: Lot Numbers: T7F017X T7J023X T7L032X T7L034X T8L100X T7F025X T7J024X T7L033X T7L035X T9F138X T7F026X T7K020X

Reason for recall

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.

FDA-determined cause: Under Investigation by firm

Action taken

Urgent Medical Device Recall notification letters dated 8/12/20 were sent to customers. Required Actions: 1.Please immediately quarantine and discontinue use of affected item codes with associated lot numbers listedon Attachment A. 2.Please return affected product as indicated below. All unused products from the affected item codes and associated lot numbers must be returned. 3.If you have distributed the Covidien Endo GIA" Auto Suture" universal articulating loading units listed on Attachment A, please promptly forward the information from this letter to those recipients. 4.Complete the Recalled Product Return Form even if you do not have inventory. We regret any inconvenience this may cause. We are committed to patient safety and appreciate your prompt attention to this matter. If you have any questions regarding this communication, please contact your Medtronic representative or Customer Service at 800-962-9888, option 2.

Details

Recall number
Z-0004-2021
Initiated
August 12, 2020
Product code
GDW – Staple, Implantable
Quantity
900,007 total
Distribution
Worldwide distribution - US Nationwide and Global Distribution.
Recalling firm
Covidien, LP, North Haven, CT

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0001-2021 Class IIEndo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0002-2021 Class IIEndo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm, Item Code…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0003-2021 Class IIEndo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm, Item Code…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0005-2021 Class IIEndo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm, Item Code 030454 - Product…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0006-2021 Class IIEndo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm, Item Code…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0007-2021 Class IIEndo GIA Auto Suture Universal Loading Unit, Item Code 030457 - Product Usage: The Endo…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0008-2021 Class IIEndo GIA Auto Suture Universal Articulating Loading Unit 60 mm - 3.5 mm, Item Code…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified
Z-0009-2021 Class IICovidien Best Practices Procedure Kits containing Auto Suture Endo GIA Universal Loading…The device staples may not properly form upon application preventing adequate hemostasis. Use of a product… 08/12/2020Open, Classified