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fda_recall · device_recall · high

Biomet, Inc. — Class II recall: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product De…

Event date
2026-08-12 00:00:00Z
Observed
2026-08-19 04:20:41Z
Source ID
Z-2868-2026
Payload hash
1d469b5779e4ba0ad739fc60

Summary

Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade. Status: Ongoing.

Entities

Frequently asked questions

Has Biomet, Inc. had other FDA enforcement actions?
Yes. Argus HQ has recorded 5 total FDA actions tied to Biomet, Inc.: 0 warning letters, 5 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 2026-08-12; Argus observed and indexed it on 2026-08-19.
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). Biomet, Inc. — Class II recall: Intramedullary Bone Saw Blade Assembly  Model/Catalog Number: 475625  Product De…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-biomet-inc-z-2868-2026
MLA
"Biomet, Inc. — Class II recall: Intramedullary Bone Saw Blade Assembly  Model/Catalog Number: 475625  Product De…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-biomet-inc-z-2868-2026.
Chicago
Argus HQ Research. "Biomet, Inc. — Class II recall: Intramedullary Bone Saw Blade Assembly  Model/Catalog Number: 475625  Product De…." Digital Empire Holdings LLC. Accessed August 19, 2026. https://argushq.ai/events/fda-recall-biomet-inc-z-2868-2026.
BibTeX
@misc{argushq_argushq_ai_events_fda_recall_biomet_inc_z_2868_2026_2026,
  title = {Biomet, Inc. — Class II recall: Intramedullary Bone Saw Blade Assembly  Model/Catalog Number: 475625  Product De…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-biomet-inc-z-2868-2026},
  note = {Accessed: August 19, 2026}
}

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