Has Stryker Spine had other FDA enforcement actions?

Yes. Argus HQ has recorded 6 total FDA actions tied to Stryker Spine: 0 warning letters, 6 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 2023-12-27; 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

Stryker Spine — Class II recall: LITe Decompression Snake Arm, REF 48080230

Name: FDA Recall Record — Stryker Spine
Creator: Argus HQ
Published: 2023-12-27
License: https://argushq.ai/methodology

Event date: 2023-12-27 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-0610-2024
Payload hash: 843ff0efe4653c0e53bc9679…

Summary

Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft. Status: Ongoing.

Entities

Stryker Spine

View source record ↗

Frequently asked questions

Has Stryker Spine had other FDA enforcement actions?: Yes. Argus HQ has recorded 6 total FDA actions tied to Stryker Spine: 0 warning letters, 6 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 2023-12-27; 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 (2023). Stryker Spine — Class II recall: LITe Decompression Snake Arm, REF 48080230. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-stryker-spine-z-0610-2024

MLA

"Stryker Spine — Class II recall: LITe Decompression Snake Arm, REF 48080230." Argus HQ Research, Digital Empire Holdings LLC, 2023, argushq.ai/events/fda-recall-stryker-spine-z-0610-2024.

Chicago

Argus HQ Research. "Stryker Spine — Class II recall: LITe Decompression Snake Arm, REF 48080230." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-stryker-spine-z-0610-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_stryker_spine_z_0610_2024_2023,
  title = {Stryker Spine — Class II recall: LITe Decompression Snake Arm, REF 48080230},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-stryker-spine-z-0610-2024},
  note = {Accessed: July 23, 2026}
}

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