Covidien recalls

Covidien has 493 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 26 Aug 2026. 177 are still ongoing. 15 were reported in the last 12 months.

Total recalls493since 2012
Last 12 months15reported
Class I6613% of total
Ongoing177latest 26 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 66 13%Class II 425 86%Class III 2 0%

By year

Ongoing covidien recalls

177 active

All covidien recalls, newest first

493 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEndoFLIP System that includes recalled by CovidienCovidienOtherNationwide
DeviceCLASS IIDermalon 88861757-31 Dermalon* 4-0 Blu C13 recalled by CovidienCovidienSterilityNationwide
DeviceCLASS IISurgipro SP-623 Surgipro* 2-0 BLU SC2 X36 SP recalled by CovidienCovidienSterilityNationwide
DeviceCLASS IIV-Loc 90 Absorbable Wound Closure Device Vloc 90 0 VL recalledCovidienSterilityNationwide
DeviceCLASS IISurgipro II S8698GX Surgipro II BL 5/0 18 P-13 S8698GX recalledCovidienSterilityNationwide
DeviceCLASS IIV-Loc 180 Absorbable Wound Closure Device Box Bedside recalledCovidienSterilityNationwide
DeviceCLASS IIShiley Disposable Decannulation Plug recalled by CovidienCovidienOtherNationwide
DeviceCLASS IIEndoStitch" Polysorb Single Use Loading Unit recalled by CovidienCovidienSterilityNationwide
DeviceCLASS IIMon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM recalledCovidienTemperature AbuseNationwide
DeviceCLASS IIMon-a-Therm General Purpose Temperature Probe recalled by CovidienCovidienTemperature AbuseNationwide
DeviceCLASS IIShiley Tracheostomy Tube Cuffed with Inner Cannula recalled by CovidienCovidienOtherNationwide
DeviceCLASS IIMon-a-Therm general purpose temperature probe size recalled by CovidienCovidienTemperature AbuseNationwide
DeviceCLASS IIHealthCast "Vital Sync" Remote Patient Monitoring System recalledCovidienDevice MalfunctionNationwide
DeviceCLASS IISignia" Small Diameter Curved Tip Intelligent Reload Vascular/Thin) recalledCovidienOtherNationwide
DeviceCLASS IISignia" Small Diameter Curved Tip Intelligent Reload Vascular/Thin) recalledCovidienOtherNationwide
DeviceCLASS IINellcor Bedside SpO2 Patient Monitoring System recalled by CovidienCovidienDevice MalfunctionNationwide
DeviceCLASS IShiley Adult Flexible Tracheostomy Tube recalled by CovidienCovidienDevice MalfunctionCO
DeviceCLASS IIChameleon PTA Balloon Catheter with Injection Port recalled by CovidienCovidienOtherNationwide
DeviceCLASS IMcGRATH" MAC EMS Video Laryngoscope recalled by CovidienCovidienDevice MalfunctionNationwide
DeviceCLASS IPuritan Bennett 500 Series Ventilators (Description recalled by CovidienCovidienOther34 states
DeviceCLASS IIEsoFLIP Balloon Dilation Catheter recalled by CovidienCovidienLabeling ErrorsNationwide
DeviceCLASS IITri-Staple 2.0 Black Reinforced Intelligent Reload recalled by CovidienCovidienOtherNationwide
DeviceCLASS IISofsilk Braided Silk sutures, Product Number S-2782K recalledCovidienSterilityCT
DeviceCLASS IIMedtronic Invos, Reusable Sensor Cable for PM7100 recalled by CovidienCovidienDevice Malfunction22 states
DeviceCLASS IIMedtronic Invos, Reusable Infant Sensor Adapter Cable for PM7100 recalledCovidienDevice Malfunction22 states
DeviceCLASS IIPalindrome Precision H Chronic Catheter Kit 14./Ch recalled by CovidienCovidienDevice MalfunctionNationwide
DeviceCLASS IIPalindrome Precision HSI Chronic Catheter Sport Pack 14./Ch recalledCovidienDevice MalfunctionNationwide
DeviceCLASS IIAuto Suture" Blunt Tip Trocar, Product Number OMS-T10BTS recalledCovidienPackaging DefectsNationwide
DeviceCLASS IIAuto Suture" Structural Balloon Trocar, Product Number OMS-T10SB recalledCovidienPackaging DefectsNationwide
DeviceCLASS IIAuto Suture" Blunt Tip Trocar, Product Number OMS-T10BTNL recalledCovidienPackaging DefectsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.