K2M recalls

K2M has 39 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 6 Jul 2022. 3 are still ongoing. The most frequent reason is device malfunction.

Total recalls39since 2019
Last 12 months0reported
Class I00% of total
Ongoing3latest 6 Jul 2022

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 39 100%Class III 0 0%

By year

Ongoing k2m recalls

3 active
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIYukon Straight Rod recalled by K2MK2MOther6 states
DeviceCLASS IIEverest MI XT Outer Dilator recalled by K2MK2MOtherNationwide
DeviceCLASS IIEverest MI XT Inner Dilator recalled by K2MK2MOtherNationwide

All k2m recalls, newest first

39 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIYukon Straight Rod recalled by K2MK2MOther6 states
DeviceCLASS IIEverest MI XT Outer Dilator recalled by K2MK2MOtherNationwide
DeviceCLASS IIEverest MI XT Inner Dilator recalled by K2MK2MOtherNationwide
DeviceCLASS IIChesapeake Anterior Lumbar (AL) Removal Tool recalled by K2MK2MOther9 states
DeviceCLASS IICascadia AN Interbody Convex 10x22x14mm recalled by K2MK2MLabeling ErrorsNationwide
DeviceCLASS IICascadia AN Interbody Convex 10x22x15mm recalled by K2MK2MLabeling ErrorsNationwide
DeviceCLASS IICascadia AN Interbody Convex 10x28x14mm recalled by K2MK2MLabeling ErrorsNationwide
DeviceCLASS IIChesapeake Cervical-Ti Drill Guide Inserter- a multi-screw recalledK2MPotency & AssayPA
DeviceCLASS IIYukon Polyaxial Screw Size 4.0x26mm recalled by K2MK2MOtherNationwide
DeviceCLASS IIEverest MI XT Tab Removal Tool (i.e recalled by K2MK2MForeign MaterialNationwide
DeviceCLASS IIYukon OCT Spinal System Yukon Anti-Torque Alignment Tube recalled by K2MK2MOtherNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide
DeviceCLASS IIAleutian Interbody Spacer Systems, EN AN Lordotic Spreader recalledK2MDevice MalfunctionNationwide

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.