PlainRecalls

Howmedica Osteonics Corp.

Compiled from official public sources by the publisher.

232 recalls on record · Latest: Jun 24, 2026

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Agency notice ledger

Federal filing book Howmedica Osteonics Corp. HEAVY-BOOK · SINGLE-AGENCY

#56 of 14,151 · 232 notices · 0.222% archive

  • BOOK 232 notices
  • RANK #56 of 14,151
  • SHARE 0.222% archive
  • AGENCY FDA Devices (232)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jun 24, 2026
  • PHOTO Dole Fresh Vegetables…

Nearest notice-volume peer: Dole Fresh Vegetables Inc (2 notice gap)

Howmedica Osteonics Corp. accounts for about 0.222% of the 104,423-notice archive on 232 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 →

Where Howmedica Osteonics Corp. sits among 14,151 recalling firms

Howmedica Osteonics Corp. ranks 56th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Howmedica Osteonics Corp. vs all firms by recall-notice count

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

232 56th of 14151 higher than 14,095 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

Howmedica Osteonics Corp. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Howmedica Osteonics Corp. holds about 0.222% of archive notices alongside 232 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 23, 2022

Simplex HV With Gentamicin CE, 10 PACK-Bone cement with Gentomycin Catalog Number: 6193-1-010
FDA Devices Moderate Oct 5, 2022

Short tibial bearing MK4 - Std, STM, Catalog No. SMMLTB02. Knee prosthesis component.
FDA Devices Moderate Jun 15, 2022

Triathlon Tritanium Tibial Component (Size 6); Catalog Number 5536-B-600 Triathlon¿ Tritanium¿ Tibial Component (Size 5); Catalog Number 5536-B-500
FDA Devices Moderate Apr 6, 2022

Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
FDA Devices Moderate Apr 6, 2022

Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032
FDA Devices Moderate Feb 23, 2022

32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
FDA Devices Moderate Feb 23, 2022

Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
FDA Devices Moderate Feb 23, 2022

Dall Miles SM GRIP AND 2 1.6MM HOMOG CBL, Catalog Number 6704-0-110
FDA Devices Moderate Feb 23, 2022

Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044
FDA Devices Moderate Jan 12, 2022

Triathlon Pro Tibial Preparation Tray, Revision AC- for organization, storage, and transport in preparation for sterilization of re-usable instruments required for implanting the Triathlon Globalization Implant System for individual patients receiving primary total knee arthroplasty (TKA). Catalog# 6541-9-109
FDA Devices Moderate Dec 8, 2021

28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
FDA Devices Moderate Dec 8, 2021

28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
FDA Devices Moderate Aug 25, 2021

Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700
FDA Devices Moderate Apr 14, 2021

Trial Cutting Guide for Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System, prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer. Catalog Number: I-K3834CG00 Specialty Triathlon TS Trial Cutting Guide Set I-K3834CG1L Specialty Triathlon TS Trial Cutting Guide Size 1 Left I-K3834CG1R Specialty Triathlon TS Trial Cutting Guide Size 1 Right I-K3834CG2L Specialty Triathlon TS Trial Cutting Guide Size 2 Left

FDA Devices Moderate Mar 17, 2021

Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Right, Sterile, Catalog # 504-02-54C-R, UDI (01)07613327012415(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 64 left, Sterile, Catalog # 504-02-64E-L, UDI (01)07613327012484(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 56 Right, Sterile, Catalog # 504-02-56D-R, UDI (01)07613327012347(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Left, Sterile, Catalog # 504-02-54C-L, UDI (01)07613327012354(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 60 right, Sterile, Catalog # 504-02-60D-R, UDI (01)07613327012408(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 62 right, Sterile, Catalog # 504-02-62E-R, UDI (01)07613327012439(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 60 Left, Sterile, Catalog # 504-02-60D-L, UDI (01)07613327012422(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 56 Left, Sterile, Catalog # 504-02-56D-L, UDI (01)07613327012361(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 62 left, Sterile, Catalog # 504-02-62E-L, UDI (01)07613327012453(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 64 right, Sterile, Catalog # 504-02-64E-R, UDI (01)07613327012460(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 58 Left, Sterile, Catalog # 504-02-58D-L, UDI (01)07613327012385(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 58 Right, Sterile, Catalog # 504-02-58D-R, UDI (01)07613327012446(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 66 right, Sterile, Catalog # 504-02-66F-R, UDI (01)07613327012477(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 68 left, Sterile, Catalog # 504-02-68F-L, UDI (01)07613327012521(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 66 left, Sterile, Catalog # 504-02-66F-L, UDI (01)07613327012491(17)
FDA Devices Moderate May 27, 2020

Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 68 right, Sterile, Catalog # 504-02-68F-R, UDI (01)07613327012514(17)
FDA Devices Moderate May 13, 2020

Cortoss Bone Augmentation Material, Catalog Nos. 2101-0005 and 2101-0010
FDA Devices Moderate Jan 22, 2020

Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
FDA Devices Moderate Dec 4, 2019

Stryker X-Change Medial Wall Mesh Small (6-Petal)-Intended to be implanted to replace a hip joint REF 0942-8-025
FDA Devices Moderate Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 RIGHT Catalog # 5542-A-202 - Product Usage: Triathlon Femoral Distal Augments are used with Triathlon TS Femoral Components during revision Total Knee Arthroplasty (TKA) and with Triathlon Primary PS Femoral Components during TKA to address distal femoral defects. (See attached IFU (IFU_Triathlon Total Knee_QIN 4376 Rev AB).
FDA Devices Moderate Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 15MM - SIZE 2 LEFTTriathlon Femoral Distal Augments are used with Triathlon TS Femoral Components during revision Total Knee Arthroplasty (TKA) and with Triathlon Primary PS Femoral Components during TKA to address distal femoral defects. (See attached IFU (IFU_Triathlon Total Knee_QIN 4376 Rev AB) Catalog # 5542-A-201 - Product Usage:
FDA Devices Moderate Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 LEFT Catalog # 5541-A-201 - Product Usage: Triathlon Femoral Distal Augments are used with Triathlon TS Femoral Components during revision Total Knee Arthroplasty (TKA) and with Triathlon Primary PS Femoral Components during TKA to address distal femoral defects. (See attached IFU (IFU_Triathlon Total Knee_QIN 4376 Rev AB).
FDA Devices Moderate Oct 9, 2019

TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog # 5541-A-202 - Product Usage: Triathlon Femoral Distal Augments are used with Triathlon TS Femoral Components during revision Total Knee Arthroplasty (TKA) and with Triathlon Primary PS Femoral Components during TKA to address distal femoral defects. (See attached IFU (IFU_Triathlon Total Knee_QIN 4376 Rev AB).
FDA Devices Moderate Aug 14, 2019

Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato 9.5mm X 100mm Polyaxial Screw Catalog Number 4826195100
FDA Devices Moderate Jan 2, 2019

HydroSet XT Injectable HA Bone Cement, REF 897003, STERILE
FDA Devices Moderate Jan 2, 2019

HydroSet XT Injectable HA Bone Cement, REF 897005, STERILE
FDA Devices Moderate Dec 26, 2018

Reliance LITe Nerve Hook Bayoneted, 90, Blunt Tip, REF # 48066103 The blunt probe can be used as a conventional means of achieving nerve retraction. The bend at the proximal tip of the ring the discectomy, as well as during the insertion of an IBD during a conventional TLIF procedure.
FDA Devices Moderate Dec 19, 2018

Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and minimally invasive PLIF or TLIF surgical procedure.
FDA Devices Moderate Nov 14, 2018

Sterile Knee Instruments Disposable Fluted Headless Pins, DIA 3.2mm LNTH 89mm, REF 7650-2038A - Product Usage: Howmedica Osteonics Corp. (Stryker, Joint Reconstructive Division) Sterile Instrumentation consists of manual surgical instrumentation intended for use during hip, knee, shoulder, elbow or wrist arthroplasty, or trauma surgeries.
FDA Devices Moderate Oct 31, 2018

Tritanium TL Steerable Inserter, Cat. No. 48930000, UDI 07613327381900 Product Usage: The TL Steerable Inserter is a Class 1 instrument which is provided in a non-sterile condition. The inserter is designed to enter the disc space, with a fixed engagement between the inserter and the cage and then rotate for desired placement. The three components of the TL Steerable Inserter System include: 1. TL Steerable Inserter 2. TL Steerable Inserter Inner Shaft 3. TL Steerable Inserter Driver
FDA Devices Moderate Aug 15, 2018

radial stem implant #3 (Sterile packed). Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.
FDA Devices Moderate Aug 15, 2018

Radio Capitellum Small, Left. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.
FDA Devices Moderate Aug 15, 2018

Lateral Assembly, Radial Head Impl Assembly, Size 4. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.
FDA Devices Moderate Aug 15, 2018

rHead Recon Stem Implant non-coated, Size 1. Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.
FDA Devices Moderate Aug 15, 2018

#4 Bipolar radial head Implant (Sterile packed). Orthopedic implant for replacement of the proximal end of the radius in the Stryker rHead Radial Head and Uni-Elbow system.

Howmedica Osteonics Corp. carries an outsized archive share

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

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

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Frequently Asked Questions

How many federal recall notices name Howmedica Osteonics Corp.? ▼
PlainRecalls indexes 232 distinct federal recall events naming Howmedica Osteonics Corp., 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 Howmedica Osteonics Corp. sit among other recalling firms? ▼
Howmedica Osteonics Corp. ranks #56 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 Howmedica Osteonics Corp.'s notices? ▼
FDA Devices accounts for 232 of this firm's 232 indexed notices.
What product category dominates Howmedica Osteonics Corp.'s filing book? ▼
Filings for Howmedica Osteonics Corp. 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.
Howmedica Osteonics Corp.: 232 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 Howmedica Osteonics Corp.; individual notices remain authoritative on each linked recall page.

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