Has Stryker Neurovascular had other FDA enforcement actions?

Yes. Argus HQ has recorded 14 total FDA actions tied to Stryker Neurovascular: 0 warning letters, 14 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 2024-06-12; 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 Neurovascular — Class II recall: The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip an…

Name: FDA Recall Record — Stryker Neurovascular
Creator: Argus HQ
Published: 2024-06-12
License: https://argushq.ai/methodology

Event date: 2024-06-12 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1941-2024
Payload hash: cd6b4d67b65e99cbbf1dcfd3…

Summary

Stryker Neurovascular has observed an increased frequency of PTFE coating damage occurring on the Synchro Guidewires that may be caused by the practice of backloading the guidewire through the optional introducer accessory. This issue is limited to certain lots of the Synchro Guidewire that contain… Status: Ongoing.

Entities

Stryker Neurovascular

View source record ↗

Frequently asked questions

Has Stryker Neurovascular had other FDA enforcement actions?: Yes. Argus HQ has recorded 14 total FDA actions tied to Stryker Neurovascular: 0 warning letters, 14 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 2024-06-12; 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). Stryker Neurovascular — Class II recall: The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip an…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-stryker-neurovascular-z-1941-2024

MLA

"Stryker Neurovascular — Class II recall: The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip an…." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-stryker-neurovascular-z-1941-2024.

Chicago

Argus HQ Research. "Stryker Neurovascular — Class II recall: The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip an…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-stryker-neurovascular-z-1941-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_stryker_neurovascular_z_1941_2024_2024,
  title = {Stryker Neurovascular — Class II recall: The Synchro2 Guidewires are a steerable guidewire family with a shapeable tip an…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-stryker-neurovascular-z-1941-2024},
  note = {Accessed: July 23, 2026}
}

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