Stryker Spine recalls

Stryker Spine has 29 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 9 Apr 2025. 6 are still ongoing.

Total recalls29since 2012
Last 12 months0reported
Class I13% of total
Ongoing6latest 9 Apr 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 3%Class II 28 97%Class III 0 0%

Why stryker spine is recalled

By year

Ongoing stryker spine recalls

6 active

All stryker spine recalls, newest first

29 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIMonterey AL Implant Inserter recalled by Stryker SpineStryker SpineOther13 states
DeviceCLASS IIMonterey AL Implant Inserter recalled by Stryker SpineStryker SpineOther13 states
DeviceCLASS IIMonterey AL Implant Inserter recalled by Stryker SpineStryker SpineOther13 states
DeviceCLASS IIMonterey AL Implant Inserter recalled by Stryker SpineStryker SpineOther13 states
DeviceCLASS IIAVS Anchor-C Cervical Cage System Instructions For Use recalledStryker SpineOtherNationwide
DeviceCLASS IILITe Decompression Snake Arm recalled by Stryker SpineStryker SpineOther4 states
DeviceCLASS IICortoss Bone Augmentation Material 10cc Cartridge recalledStryker SpineTemperature AbuseNationwide
DeviceCLASS IICortoss Bone Augmentation Material 5cc Cartridge recalledStryker SpineTemperature AbuseNationwide
DeviceCLASS IITritanium X TL Instruments - intervertebral fusion device recalledStryker SpineDevice MalfunctionNationwide
DeviceCLASS IIAVS Aria Cage recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IIAccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF recalledStryker SpineOtherNationwide
DeviceCLASS IIStryker Aero-AL Impaction handle recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IIStryker Radius 5.5 to 3.5 Rod to Red Connector recalled by Stryker SpineStryker SpineDevice MalfunctionNationwide
DeviceCLASS IIStryker UniVise Spinous Process Fixation Plate System recalledStryker SpineOtherNationwide
DeviceCLASS IISpecialty Audible Torque Wrench recalled by Stryker SpineStryker SpineOther8 states
DeviceCLASS IISpecialty Aria Inserter recalled by Stryker SpineStryker SpineDevice Malfunction23 states
DeviceCLASS IIStryker Aria Implant Inserter recalled by Stryker SpineStryker SpineDevice Malfunction23 states
DeviceCLASS IISpecialty Straight Static Inserter Assembly recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IIStryker XIA Torque Wrench XIA 3 Torque Wrench XIA Elegance recalledStryker SpineOtherNationwide
DeviceCLASS IStryker Oasys Midline Occiput Plate-1) Small Medium Large Long Mini recalledStryker SpineOtherNationwide
DeviceCLASS IIStryker XIA 3 Iliac Screwdriver The XIA 3 Iliac Screwdriver recalledStryker SpineOtherNationwide
DeviceCLASS IIStryker Xia 3 Torque Wrench recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IIStryker Mantis Torque Wrench recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IISpecialty Audible Torque Wrench, Xia Is2217xlp recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IIAviator Drill Bit recalled by Stryker SpineStryker SpineOtherNationwide
DeviceCLASS IIThe Instructions For Use for the following recalled by Stryker SpineStryker SpineSterilityGA
DeviceCLASS IIStryker Reliance AL Implant Blocker recalled by Stryker SpineStryker SpineDevice MalfunctionNationwide
DeviceCLASS IILuxor Retractor Base recalled by Stryker SpineStryker SpineOtherNJ
DeviceCLASS IIStryker AVS Navigator Trials recalled by Stryker SpineStryker SpineOtherNationwide

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.