PlainRecalls

DePuy Orthopaedics, Inc.

Compiled from official public sources by the publisher.

155 recalls on record · Latest: Apr 10, 2024

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Agency notice ledger

Federal filing book DePuy Orthopaedics, Inc. HEAVY-BOOK · SINGLE-AGENCY

#102 of 14,151 · 155 notices · 0.148% archive

  • BOOK 155 notices
  • RANK #102 of 14,151
  • SHARE 0.148% archive
  • AGENCY FDA Devices (155)
  • CAT medical devices
  • CATS 1 category
  • LATEST Apr 10, 2024
  • PHOTO Dodge

Nearest notice-volume peer: Dodge (2 notice gap)

DePuy Orthopaedics, Inc. accounts for about 0.148% of the 104,423-notice archive on 155 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How DePuy Orthopaedics, Inc. compares to 14,151 recalling firms

DePuy Orthopaedics, Inc. ranks 102nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

DePuy Orthopaedics, Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

155 102nd of 14151 higher than 14,049 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

DePuy Orthopaedics, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows DePuy Orthopaedics, Inc. holds about 0.148% of archive notices alongside 155 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Apr 10, 2024

ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology, Size 6. Component of the ATTUNE Total Knee Replacement System.
FDA Devices Moderate Mar 29, 2023

Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118
FDA Devices Moderate Mar 29, 2023

Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 151760312
FDA Devices Moderate Mar 29, 2023

Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760212
FDA Devices Moderate Mar 29, 2023

Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226
FDA Devices Moderate Mar 29, 2023

Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507
FDA Devices Moderate Jul 27, 2022

ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant Part Number: 254400525
FDA Devices Moderate Jul 20, 2022

MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000, 136342000, 136343000, 136344000, 136345000, 136346000, 136347000, 136348000, 136349000, 136350000, 136351000, 136352000, 136353000, 136354000, 136356000, 136358000, 136360000
FDA Devices Moderate May 11, 2022

VELYS Robotic-Assisted Solution Base Product No.: 451570100
FDA Devices Moderate Feb 16, 2022

ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154909003
FDA Devices Moderate Feb 16, 2022

ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
FDA Devices Moderate Jan 19, 2022

GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100
FDA Devices Moderate Oct 13, 2021

ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420915
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420579
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT FEM CUT TIB PIN R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420907
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420581
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420917
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420916
FDA Devices Moderate Sep 8, 2021

TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420578
FDA Devices Moderate Sep 1, 2021

ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080
FDA Devices Moderate Jun 16, 2021

DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number: 1365-21-000, Part Description: ARTICUL/EZE BALL 32 +1 GR
FDA Devices Moderate Apr 7, 2021

ATTUNE¿ FIXED BEARING KNEE - Product Usage: composed of individually packaged femoral, tibial and patellar components designed to replace the natural articular surface of the knee joint. The femoral component is a metal implant without a porous coating. The tibial component may be an all polyethylene component or comprised of a metal tibial base without porous coating, and a polyethylene insert and locking components. The patella component may be of an all polyethylene design.
FDA Devices Moderate Apr 7, 2021

The ATTUNE¿ Rotating Platform (RP) Total Knee System - Product Usage: consists of multiple components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.
FDA Devices Moderate Apr 7, 2021

The LCS COMPLETE P.F.C.TM SIGMA RP Mobile Bearing Total Knee System - Product Usage: consists of three components intended to replace the femoral, tibial, and patellar articular surfaces of the knee joint.
FDA Devices Moderate Feb 17, 2021

Universal Femoral Sleeves - Product Usage: used primarily in revision surgeries with the S-ROM Noiles, LPS, SIGMA, and LCS Knee products.
FDA Devices Moderate Jan 13, 2021

Pinnacle Cups, Part numbers 121701048 121701050 121701052 121701054 121701056 121701058 121701060 121701062 121711048 121711052 121712050 121712052 121712056 121722048 121722050 121722052 121722054 121722056 121722058 121722060 121722062 121731048 121731050 121731052 121731054 121731056 121731058 121731060 121731062 121732048 121732050 121732052 121732054 121732056 121732058 121732060 121732062 121732064 - Product Usage: The PINNACLE CUP devices are part of the Pinnacle Hip Solution for the anat
FDA Devices Moderate Feb 19, 2020

SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.
FDA Devices Moderate Apr 17, 2019

CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
FDA Devices Moderate Apr 17, 2019

CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
FDA Devices Moderate Apr 17, 2019

CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO), Pro. Code L20433 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
FDA Devices Moderate Sep 5, 2018

P.F.C. SIGMA Revision Knee System Distal Augment, Model Number 960830
FDA Devices Moderate Aug 1, 2018

CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511
FDA Devices Moderate May 16, 2018

ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee
FDA Devices Moderate May 16, 2018

ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee
FDA Devices Moderate Apr 4, 2018

(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP Cemented Trochlea Size 2 Narrow Left, Catalog Number: 102403200, GTIN: 10603295001621; (3) Sigma HP Cemented Trochlea Size 3 Narrow Left, Catalog Number: 102403300, GTIN: 10603295001638; (4) Sigma HP Cemented Trochlea Size 4 Narrow Left, Catalog Number: 102403400, GTIN: 10603295001645; (5) Sigma HP Cemented Trochlea Size 5 Narrow Left, Catalog Number: 102403500, GTIN: 10603295001652;

FDA Devices Moderate Mar 21, 2018

The GLOBAL UNITE Platform Shoulder System is intended for cemented or uncemented total shoulder or hemi-shoulder replacement procedures, Product labeling: LE¿O-1100-30-000 REV D.pdf.pdf, LE¿O-1100-40-000 REV D.pdf.pdf, LE¿O-110030100_REV D.pdf.pdf, LE¿O-110030110_REV D.pdf.pdf, LE¿O-110030120_REV D.pdf.pdf
FDA Devices Moderate Mar 14, 2018

Concorde Lift Torque Limiting Handle. Must be used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
FDA Devices Moderate Mar 14, 2018

Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
FDA Devices Moderate Mar 7, 2018

DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants intended for use in total shoulder or hemi-shoulder replacement procedures in patients with non-functional rotator cuffs. HA components are for cementless use only.
FDA Devices Moderate Mar 7, 2018

DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants are intended for use in total shoulder or hemi-shoulder replacement procedures in patients with non-functional rotator cuffs. HA components are for cementless use only.
FDA Devices Moderate Feb 21, 2018

CORAIL HIGH OFFSET STEM Collarless SIZE 14
FDA Devices Moderate Feb 21, 2018

CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9

DePuy Orthopaedics, Inc. carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name DePuy Orthopaedics, Inc.? ▼
PlainRecalls indexes 155 distinct federal recall events naming DePuy Orthopaedics, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does DePuy Orthopaedics, Inc. sit among other recalling firms? ▼
DePuy Orthopaedics, Inc. ranks #102 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of DePuy Orthopaedics, Inc.'s notices? ▼
FDA Devices accounts for 155 of this firm's 155 indexed notices.
What product category dominates DePuy Orthopaedics, Inc.'s filing book? ▼
Filings for DePuy Orthopaedics, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
DePuy Orthopaedics, Inc.: 155 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming DePuy Orthopaedics, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026