Covidien (Dba Medtronic)

FDA Regulatory Profile

Covidien (Dba Medtronic) has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest 510(k)
May 16, 2017

Newer recall under related name Covidien: Jun 24, 2026, Z-2922-2026.

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances1Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Covidien
Same company group
494225671Jun 24, 2026 (Z-2922-2026)
Medtronic Perfusion Systems
Same company group
11629110Jun 24, 2026 (Z-2811-2026)
Medtronic Neurosurgery
Same company group
322840Jun 17, 2026 (Z-2768-2026)
Medtronic Neuromodulation
Same company group
981152May 13, 2026 (Z-2241-2026)
Medtronic
Same company group
157248512Mar 11, 2026 (Z-1948-2026)
Mazor Robotics
Same company group
51300Dec 10, 2025 (Z-1122-2026)
Medtronic Xomed
Same company group
264770Jul 17, 2025 (Z-2461-2025)
Ev3
Same company group
113500Dec 10, 2024 (Z-0904-2025)
Medtronic Navigation
Same company group
9244121Dec 4, 2024 (Z-1022-2025)
Intersect Ent
Same company group
2160Jan 4, 2023 (D-0167-2023)
Medtronic Vascular
Same company group
230480230Mar 23, 2022 (Z-1043-2022)
Medtronic Advanced Energy
Same company group
121130Dec 28, 2016 (Z-1136-2017)

Recent 510(k) Clearances

K-NumberDeviceDate
K163002Kangaroo Feeding Tube with IRIS TechnologyMay 16, 2017