COVIDIEN MEDTRONIC Recalls — U.S. Recall Records

Recall history in this database

Classification mix: Class II: 54.

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple recall — FDA Z-2503-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling recall — FDA Z-2514-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 45mm Gray Articulating Vascular Reload with Tri-Staple recall — FDA Z-2509-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple recall — FDA Z-2511-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling recall — FDA Z-2516-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system 30 recall — FDA Z-2508-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 60 mm Articulating Medium/Thick Reload with recall — FDA Z-2504-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 60 mm Articulating Vascular/Medium Loading Unit with Tri-Staple recall — FDA Z-2506-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple recall — FDA Z-2505-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 45 mm Extra Thick Black Articulating Reload with Tri-Staple recall — FDA Z-2510-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling recall — FDA Z-2515-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system 30 recall — FDA Z-2513-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with recall — FDA Z-2512-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceJul 25, 2018

COVIDIEN MEDTRONIC Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling recall — FDA Z-2507-2018

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…

Class IIFDA: OngoingCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC BOX TGGLOGOWX1 DO TOTAL GASTRECTOMIII Product Usage: The Endo GIA recall — FDA Z-1862-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC (1)BOX HEMIGX1 ZESTAW DO HEMICOLECTOMII recall — FDA Z-1830-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC (1) BOX LAPZD ZESTAW DO SG (2) BOX LAPISG1 ZESTAW DO SG (3) BOX LAPISGW recall — FDA Z-1847-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA universal and Endo recall — FDA Z-1832-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC BOX PST03699 KIT APP MED ALTERNATIV STAP Product Usage: The Endo GIA recall — FDA Z-1854-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC BOX PST03533 KIT APP STAPLER Product Usage: The Endo GIA universal and recall — FDA Z-1852-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC BOX KIT1171C KIT LAP CYSTECTOMY Product Usage: The Endo GIA universal and recall — FDA Z-1834-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC Endo GIA" 45mm Gray Curved Tip Articulating Vascular Reload with recall — FDA Z-1823-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with recall — FDA Z-1822-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Medical DeviceMay 23, 2018

COVIDIEN MEDTRONIC BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The Endo recall — FDA Z-1825-2018

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…

Class IIFDA: TerminatedCOVIDIEN MEDTRONIC

Understanding this recall history

This page summarizes recall records in which the official source identifies COVIDIEN MEDTRONIC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.