Covidien Medical Products
FDA adverse event reports naming Covidien Medical Products as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: COVIDIEN MEDICAL PRODUCTS.
- Total reports
- 2,201
- Deaths
- 13
- Injuries
- 470
- Malfunctions
- 1,718
Reports per year
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI1,322
- Staple, ImplantableGDW292
- Pump, Infusion, EnteralLZH225
- System, Ablation, Microwave And AccessoriesNEY193
- Sleeve, Limb, CompressibleJOW113
- Device, Vascular, For Promoting EmbolizationKRD17
- Catheter, Thrombus RetrieverNRY14
- Tubes, Gastrointestinal (And Accessories)KNT6
- Pump, InfusionFRN5
- System, Image Processing, RadiologicalLLZ3
Recent recalls
- 2016-03-17TerminatedNonconforming Material/Component
Short Percutaneous Antenna with Thermosphere" Technology Standard Percutaneous Antenna with Thermosphere" Technology; The product is packaged in a blister with a tyvek lid, contained in a display box. The numbers of units per carton is 1. Long Percutaneous Antenna with Thermosphere" Technology Product Usage: The Covidien Emprint Ablation System is intended for use in percutaneous,laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of non-resectable liver tumors. The CovidienEmprint Ablation System is not intended for use in cardiac procedures
Medtronic is voluntarily recalling specific item codes and production lots of Covidien Emprint" Percutaneous Antenna with Thermosphere" Technology due to the potential for the generator to shut down in the precence of high temperature measurements in the Emprint" Percutaneous Antenna.
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