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 Aug 15, 2018

Lateral Assembly, Radial Stem Implant, Size 3. 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 Stem Implant, 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

Lateral Assembly, Radial Implant, 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

rHead Stem Implant 6mm Collar, Size 3. 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

radial stem implant #2 (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

rHead Recon Extended Stem Size 2. 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 6mm Collar, Size 2. 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 Stem Implant Plasma 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

Lat Assembly, Rad Stem Implant,Collar 6mm,Size 3. 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, Radial Implant 6 mm Collar, Size 3. 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 Standard Extended Stem, 6mm Collar, 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

Radio Capitellum Small, Right. 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 6mm Collar, 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, Radial Implant 6 mm Collar, 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

rHead Recon Stem Implant Plasma 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 8, 2018

Custom Made Implant System with Minimum Invasive Grower (MIG) component
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, 6260-9-036
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-044
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-336
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-144
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-140
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236
FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-136
FDA Devices Moderate May 2, 2018

Knee Prosthesis, Sterile, Single-Use devices Product Usage: The knee system devices are intended for use in revision total knee arthroplasty to alleviate pain and restore function
FDA Devices Moderate May 2, 2018

Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee system devices are sterile, single-use devices intended for us in revision total knee arthroplasty to alleviate pain and restore function.
FDA Devices Moderate Mar 21, 2018

Accolade and Restoration hip product; Catalog Number: 6720-0837 and 6721-0737
FDA Devices Moderate Mar 21, 2018

Accolade and Restoration hip product; Catalog Number: 6021-0030, 6276-1-127, 6276-5-216, 6020-2530, 6020-4535, 6021-0740, 6021-0230, and 6021-4535
FDA Devices Moderate Mar 7, 2018

AccuLIF TL Insertion Handle The AccuLIF Insertion Handle attaches to the implant and is specifically designed to allow a surgeon to insert the implant into the disc space with a fixed engagement between the two components to permit a controlled positioning of the implant in the anterior portion of the intervertebral space, and then through activation of the rotational pivot between the Handle and implant for final placement of the crescent-shaped cage across the anterior portion of the disc

FDA Devices Moderate Sep 21, 2016

AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an adjunct to fusion in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and

FDA Devices Moderate Sep 21, 2016

AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an adjunct to fusion in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and
FDA Devices Moderate Sep 21, 2016

AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an adjunct to fusion in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and r

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