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 Jun 24, 2026

TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
FDA Devices Moderate Jun 24, 2026

TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
FDA Devices Moderate Mar 25, 2026

MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
FDA Devices Moderate Dec 31, 2025

The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diodes (LEDs) as well as an electronics control unit for the LEDs which includes its own battery power supply. The measured LED positions can be used in one of three different modes of operation: Patient tracking, Registration using surface matching, and Automatic intra-operative mask registration.
FDA Devices Moderate Oct 8, 2025

1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352;
FDA Devices Moderate Oct 16, 2024

MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063
FDA Devices Moderate Oct 16, 2024

Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications during primary and revision Total Knee Arthroplasty (TKA) when the Triathlon Knee System is selected for use. Catalog Number: 5521-B-200
FDA Devices Moderate Sep 4, 2024

Custom Made Device - GMRS EXTENSION Piece 40MM LEFT, 35 Deg EXT Rotated Tabs (Patient Specific); Catalog Number: C-MM100434-00;
FDA Devices Moderate Jul 24, 2024

UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-043
FDA Devices Moderate Jul 24, 2024

UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-038
FDA Devices Moderate Jul 24, 2024

UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in partial hip arthroplasty. Catalog Number: 6942-5-042
FDA Devices Moderate Jun 26, 2024

Gray Revision Instrument System Accessory Tray/Case, Catalog/Part Number: 6210-9-910
FDA Devices Moderate Jun 26, 2024

HRIS Storage & Sterilization Case and Tray, Catalog/Part Number: 6210-9-900
FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E
FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-64H
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F
FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B
FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E
FDA Devices Moderate Mar 13, 2024

NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
FDA Devices Moderate Mar 13, 2024

X3 TRIATHLON CS INSERT NO 6 10 MM
FDA Devices Moderate Mar 13, 2024

X3 TRIATHLON CS INSERT NO 3 10 MM
FDA Devices Moderate Mar 13, 2024

NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM
FDA Devices Moderate Mar 13, 2024

X3 TRIATHLON CS INSERT NO 7 9 MM
FDA Devices Moderate Mar 13, 2024

X3 TRIATHLON CS INSERT NO 6 11 MM
FDA Devices Moderate Mar 13, 2024

NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
FDA Devices Moderate Mar 13, 2024

NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM
FDA Devices Moderate Feb 14, 2024

HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip arthroplasty
FDA Devices Moderate Feb 14, 2024

HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use, sterile surgical instruments used during hip arthroplasty
FDA Devices Moderate Feb 7, 2024

Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910
FDA Devices Moderate Feb 7, 2024

PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031
FDA Devices Moderate Feb 7, 2024

PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411
FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-0110
FDA Devices Moderate Feb 7, 2024

LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631
FDA Devices Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-2910
FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-2710
FDA Devices Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110
FDA Devices Moderate Feb 7, 2024

DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911
FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026
FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028
FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032
FDA Devices Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321
FDA Devices Moderate Feb 7, 2024

LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028

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.

Resource Optimization & Innovation LLC 228 Stryker Endoscopy 238 DeRoyal Industries Inc 226 Biomet 3i, LLC 222

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