DePuy Orthopaedics recalls

DePuy Orthopaedics has 153 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 10 Apr 2024. 8 are still ongoing.

Total recalls153since 2012
Last 12 months0reported
Class I53% of total
Ongoing8latest 10 Apr 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 5 3%Class II 147 96%Class III 1 1%

By year

Ongoing depuy orthopaedics recalls

8 active

All depuy orthopaedics recalls, newest first

153 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIAttune Affixium Cementless Fixed Bearing Knee recalledDePuy OrthopaedicsLabeling ErrorsNationwide
DeviceCLASS IIAttune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIAttune Revision Limb Preservation System (LPS) Tibial Insert XSM recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIAttune Revision Limb Preservation System (LPS) Tibial Insert XSM recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIAttune Revision Limb Preservation System (LPS) Tibial Insert SM recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIAttune Revision Limb Preservation System (LPS) Tibial Insert XXSM recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIAttune Measured Sizing and Rotation Guide-to size the femur recalledDePuy OrthopaedicsForeign MaterialNationwide
DeviceCLASS IIModular Cathcart Fracture Head Hip Ball, sizes to inclusive recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIVelys Robotic-Assisted Solution Base Product No. recalledDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIAttune Revision Distal Femoral Augment SZ 6- Intended as recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIAttune Revision Posterior Femoral Augment SZ 9-intended as recalledDePuy OrthopaedicsOtherNationwide
DeviceCLASS IIGlobal Unite Std Stem Sz recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Std Stem Sz recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Std Stem SZ 14 Product recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Rev Stem Sz recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Std Stem SZ 12 Product recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Std Stem Sz recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Std Stem SZ 16 Product recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIGlobal Unite Rev Stem SZ 10 Product recalled by DePuy OrthopaedicsDePuy OrthopaedicsDevice MalfunctionNationwide
DeviceCLASS IIAttune Revision Tibial Augment Size 7/8- intended recalledDePuy OrthopaedicsPackaging DefectsNationwide
DeviceCLASS IITrumatch CT Pin Guide Kit L- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IITrumatch CT Cut Guide Kit R- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IITrumatch CT Cut Guide Fem L- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IITrumatch CT Pin Guide Fem R- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IITrumatch CT FEM CUT TIB PIN R- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IITrumatch CT Pin Guide Kit R- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IITrumatch CT Cut Guide Kit L- TruMatch Patient Specific recalledDePuy OrthopaedicsNitrosamine Impurity10 states
DeviceCLASS IIAttune Revision Cemented Stem 16X80MM-intended for use recalledDePuy OrthopaedicsPackaging DefectsIN
DeviceCLASS IIDePuy Synthes Articul/eze Femoral Head recalled by DePuy OrthopaedicsDePuy OrthopaedicsForeign Material21 states
DeviceCLASS IIThe Lcs Complete P.F.C.TM Sigma RP Mobile Bearing Total Knee System recalledDePuy OrthopaedicsPackaging 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.