Has Howmedica Osteonics Corp. had other FDA enforcement actions?

Yes. Argus HQ has recorded 14 total FDA actions tied to Howmedica Osteonics Corp.: 0 warning letters, 14 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-06-24; Argus observed and indexed it on 2026-07-09.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Howmedica Osteonics Corp. — Class II recall: TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.

Name: FDA Recall Record — Howmedica Osteonics Corp.
Creator: Argus HQ
Published: 2026-06-24
License: https://argushq.ai/methodology

Event date: 2026-06-24 00:00:00Z
Observed: 2026-07-09 22:52:05Z
Source ID: Z-2462-2026
Payload hash: 4b64ecfce1b7149501177559…

Summary

Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon Universal Baseplate Size 4 (lot TYX7OB), is contained in packaging labeled as Triathlon Universal Baseplate Size 3, (lo… Status: Ongoing.

Entities

Howmedica Osteonics Corp.

View source record ↗

Frequently asked questions

Has Howmedica Osteonics Corp. had other FDA enforcement actions?: Yes. Argus HQ has recorded 14 total FDA actions tied to Howmedica Osteonics Corp.: 0 warning letters, 14 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-06-24; Argus observed and indexed it on 2026-07-09.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Howmedica Osteonics Corp. — Class II recall: TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-howmedica-osteonics-corp-z-2462-2026

MLA

"Howmedica Osteonics Corp. — Class II recall: TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-howmedica-osteonics-corp-z-2462-2026.

Chicago

Argus HQ Research. "Howmedica Osteonics Corp. — Class II recall: TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.." Digital Empire Holdings LLC. Accessed September 29, 2026. https://argushq.ai/events/fda-recall-howmedica-osteonics-corp-z-2462-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_howmedica_osteonics_corp_z_2462_2026_2026,
  title = {Howmedica Osteonics Corp. — Class II recall: TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-howmedica-osteonics-corp-z-2462-2026},
  note = {Accessed: September 29, 2026}
}

Informational only. Not legal, financial, or medical advice.