Covidien Medtronic recalls

Covidien Medtronic appears in 55 official U.S. recall notices indexed by RecallRadar.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-s…
  FDA Device · Class II · 2018-05-23 · Covidien Medtronic
  Reason: Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal content…
• Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm ( Item Code 030450) Product Usage: The Endo GIA universal and Endo G…
  FDA Device · Class II · 2018-05-23 · Covidien Medtronic
  Reason: Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal content…
• BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titan…
  FDA Device · Class II · 2018-05-23 · Covidien Medtronic
  Reason: Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal content…
• BOX MGBGLOGX1 ZESTAW MINI GASTRIC BYPASS Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-stagger…
  FDA Device · Class II · 2018-05-23 · Covidien Medtronic
  Reason: Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal content…
• Valleylab Laparoscopic Handset
  FDA Device · Class II · 2017-04-26 · Covidien Medtronic
  Reason: Customer reports of the device handset continuing to operate after release of the activation button.