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 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 41 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 7, 2024 to Mar 25, 2026.

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 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 diod…

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 Tota…

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

FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030

FDA Devices Moderate Feb 7, 2024

DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609

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.