Has Stryker Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 89 total FDA actions tied to Stryker Corporation: 0 warning letters, 89 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 2025-01-15; 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 Corporation — Class II recall: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000) 120V NEPTUNE S ROVER (0711-001-000…

Name: FDA Recall Record — Stryker Corporation
Creator: Argus HQ
Published: 2025-01-15
License: https://argushq.ai/methodology

Event date: 2025-01-15 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-0807-2025
Payload hash: 4ae9b2aad1626b1e55c158cc…

Summary

Bolts on the vacuum pump filter housing and the flange plate were not properly tightened, impacting the function of the Neptune rovers. Systems with loose bolts may fail to provide sufficient suction force or loss of suction during a procedure. Status: Ongoing.

Entities

Stryker Corporation

View source record ↗

Frequently asked questions

Has Stryker Corporation had other FDA enforcement actions?: Yes. Argus HQ has recorded 89 total FDA actions tied to Stryker Corporation: 0 warning letters, 89 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 2025-01-15; 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 (2025). Stryker Corporation — Class II recall: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000)  120V NEPTUNE S ROVER (0711-001-000…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-stryker-corporation-z-0807-2025

MLA

"Stryker Corporation — Class II recall: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000)  120V NEPTUNE S ROVER (0711-001-000…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-stryker-corporation-z-0807-2025.

Chicago

Argus HQ Research. "Stryker Corporation — Class II recall: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000)  120V NEPTUNE S ROVER (0711-001-000…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-stryker-corporation-z-0807-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_stryker_corporation_z_0807_2025_2025,
  title = {Stryker Corporation — Class II recall: 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000)  120V NEPTUNE S ROVER (0711-001-000…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-stryker-corporation-z-0807-2025},
  note = {Accessed: July 23, 2026}
}

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