Has Zimmer Biomet Spine Inc. had other FDA enforcement actions?

This is the only FDA action Argus HQ has on file for Zimmer Biomet Spine Inc. as of 2026-07-16. Argus ingests new FDA enforcement records daily.

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 2024-01-10; Argus observed and indexed it on 2026-07-16.

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

Zimmer Biomet Spine Inc. — Class II recall: Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and…

Name: FDA Recall Record — Zimmer Biomet Spine Inc.
Creator: Argus HQ
Published: 2024-01-10
License: https://argushq.ai/methodology

Event date: 2024-01-10 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-0639-2024
Payload hash: 8b46b67de25b2ba8937e6e7b…

Summary

Spinal fixation system 7.5mmx 50mm screws are packaged with the correct labeling, but the screws themselves were laser marked with an incorrect size description of 7.5 x 40; use of incorrect screws could lead to screw perforation and indention of vascular or other structures. Status: Ongoing.

Entities

Zimmer Biomet Spine Inc.

View source record ↗

Frequently asked questions

Has Zimmer Biomet Spine Inc. had other FDA enforcement actions?: This is the only FDA action Argus HQ has on file for Zimmer Biomet Spine Inc. as of 2026-07-16. Argus ingests new FDA enforcement records daily.
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 2024-01-10; Argus observed and indexed it on 2026-07-16.
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 (2024). Zimmer Biomet Spine Inc. — Class II recall: Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-zimmer-biomet-spine-inc-z-0639-2024

MLA

"Zimmer Biomet Spine Inc. — Class II recall: Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and…." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-zimmer-biomet-spine-inc-z-0639-2024.

Chicago

Argus HQ Research. "Zimmer Biomet Spine Inc. — Class II recall: Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-zimmer-biomet-spine-inc-z-0639-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_zimmer_biomet_spine_inc_z_0639_2024_2024,
  title = {Zimmer Biomet Spine Inc. — Class II recall: Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-zimmer-biomet-spine-inc-z-0639-2024},
  note = {Accessed: July 17, 2026}
}

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