Has Stryker GmbH had other FDA enforcement actions?

Yes. Argus HQ has recorded 9 total FDA actions tied to Stryker GmbH: 0 warning letters, 9 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 2025-04-23; 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 GmbH — Class II recall: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;

Name: FDA Recall Record — Stryker GmbH
Creator: Argus HQ
Published: 2025-04-23
License: https://argushq.ai/methodology

Event date: 2025-04-23 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1620-2025
Payload hash: 7173a40cf9a366c5be5b25b0…

Summary

The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. Status: Ongoing.

Entities

Stryker GmbH

View source record ↗

Frequently asked questions

Has Stryker GmbH had other FDA enforcement actions?: Yes. Argus HQ has recorded 9 total FDA actions tied to Stryker GmbH: 0 warning letters, 9 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 2025-04-23; 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 GmbH — Class II recall: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-stryker-gmbh-z-1620-2025

MLA

"Stryker GmbH — Class II recall: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-stryker-gmbh-z-1620-2025.

Chicago

Argus HQ Research. "Stryker GmbH — Class II recall: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-stryker-gmbh-z-1620-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_stryker_gmbh_z_1620_2025_2025,
  title = {Stryker GmbH — Class II recall: Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-stryker-gmbh-z-1620-2025},
  note = {Accessed: July 23, 2026}
}

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