DePuy Spine recalls

DePuy Spine has 36 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 13 Jul 2022. 2 are still ongoing.

Total recalls36since 2013
Last 12 months0reported
Class I00% of total
Ongoing2latest 13 Jul 2022

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 36 100%Class III 0 0%

By year

Ongoing depuy spine recalls

2 active

All depuy spine recalls, newest first

36 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIEIT CIF cage, H, 8degree, L- an intervertebral body fusion recalledDePuy SpinePackaging DefectsNationwide
DeviceCLASS IIEIT CIF cage, H, 8degree, S- an intervertebral body fusion recalledDePuy SpinePackaging DefectsNationwide
DeviceCLASS IIConcorde Lift, Lordotic Expandable Interbody Device recalledDePuy SpineOtherNationwide
DeviceCLASS IIConcorde Lift, Expandable Interbody Device recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIConfidence Plus Kit Spinal Cement System, Product Codes: 283910000 recalledDePuy SpineOtherMA
DeviceCLASS IISkyline Anterior Cervical Plate System Variable recalled by DePuy SpineDePuy SpinePackaging Defects15 states
DeviceCLASS IISkyline Anterior Cervical Plate System Variable Oversized Screw recalledDePuy SpinePackaging Defects15 states
DeviceCLASS IISkyline Anterior Cervical Plate System Constrained recalledDePuy SpinePackaging Defects15 states
DeviceCLASS IISkyline Anterior Cervical Plate System Variable recalled by DePuy SpineDePuy SpinePackaging Defects15 states
DeviceCLASS IISkyline Anterior Cervical Plate System Variable recalled by DePuy SpineDePuy SpinePackaging Defects15 states
DeviceCLASS IISkyline Anterior Cervical Plate System Constrained recalledDePuy SpinePackaging Defects15 states
DeviceCLASS IISkyline Anterior Cervical Plate System Variable recalled by DePuy SpineDePuy SpinePackaging Defects15 states
DeviceCLASS IIAegis Torque Handle recalled by DePuy SpineDePuy SpineProcessing Deviation9 states
DeviceCLASS IIExpedium Spine System/Synapse System recalled by DePuy SpineDePuy SpineDevice MalfunctionPA
DeviceCLASS IIPipeline LS Access System, 4th Dilator recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIPipeline LS Access System, 2nd Dilator recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIPipeline LS Access System, 15 Dilator recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIPipeline LS Access System, Holding Clip The Pipeline LS recalledDePuy SpineOtherNationwide
DeviceCLASS IIPipeline LS Access System, 3rd Dilator Insulated recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIConfidence Spinal Cement System 11CC Plus Kit, Product recalledDePuy SpinePackaging Defects33 states
DeviceCLASS IIConfidence Spinal Cement System 5CC Kit, Product recalled by DePuy SpineDePuy SpinePackaging Defects33 states
DeviceCLASS IIConfidence Spinal Cement System Kit, Product recalled by DePuy SpineDePuy SpinePackaging Defects33 states
DeviceCLASS IIDePuy Confidence Spinal Cement System 5CC Kit recalled by DePuy SpineDePuy SpineDevice MalfunctionNationwide
DeviceCLASS IIDePuy Confidence Spinal Cement System 7CC Kit recalled by DePuy SpineDePuy SpineDevice MalfunctionNationwide
DeviceCLASS IIDePuy Confidence Spinal Cement System Kit recalled by DePuy SpineDePuy SpineDevice MalfunctionNationwide
DeviceCLASS IIDePuy Confidence Spinal Cement System 11C Plus Kit recalledDePuy SpineDevice MalfunctionNationwide
DeviceCLASS IIViper Poly Screw 5.5 10 Tl Product recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIViper Poly Screw 5.5 9 Tl Product recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIViper Poly Screw 5.5 9 Tl Product recalled by DePuy SpineDePuy SpineOtherNationwide
DeviceCLASS IIViper Poly Screw 5.5 9 Tl Product recalled by DePuy SpineDePuy 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.