PlainRecalls

Howmedica Osteonics Corp.

Compiled from official public sources by the editorial team.

230 recalls on record · Latest: Mar 25, 2026

Howmedica Osteonics Corp. Recall Insight

Howmedica Osteonics Corp. appears on 230 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.226% 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 Mar 25, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 30 entries, severity tagging shows 0 critical, 30 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 22 of 30 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 (30). The date window on this page runs from Sep 21, 2016 to Aug 15, 2018.

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 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 Un…

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-…

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 U…

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-Elbo…

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 an…

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 U…

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 He…

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…

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 H…

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 s…

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 an…

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…

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…

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 a…

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 rev…

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 im…

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 …

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…

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 a…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Howmedica Osteonics Corp. with Zimmer Biomet, Inc. →

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.