PlainRecalls

DePuy Orthopaedics, Inc.

Compiled from official public sources by the editorial team.

155 recalls on record · Latest: Apr 10, 2024

DePuy Orthopaedics, Inc. Recall Insight

DePuy Orthopaedics, Inc. appears on 155 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.152% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Apr 10, 2024, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Feb 21, 2018 to Apr 10, 2024.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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: …

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,…

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: 15…

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: 1547060…

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 …

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 …

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 i…

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 …

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 …

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 …

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…

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: AR…

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 natura…

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 pa…

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, t…

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 1…

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 C…

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 t…

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 CORAI…

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…

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 labe…

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 lumb…

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 replacemen…

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 replac…

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

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.