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 2024-05-08; 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 Distal Access Catheter is a single-lumen, braided shaft, variable stiffness…

Name: FDA Recall Record — Stryker Neurovascular
Creator: Argus HQ
Published: 2024-05-08
License: https://argushq.ai/methodology

Event date: 2024-05-08 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1740-2024
Payload hash: 39f412ccdc553cf2da36eaa1…

Summary

Stryker Neurovascular is recalling their DAC- Distal Access Catheter -038 136cm, a Distal Access Catheter by removal. The reason for the recall is: the DAC Lot #0000486382 was released with out-of-specification endotoxin results. 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 2024-05-08; 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 Distal Access Catheter is a single-lumen, braided shaft, variable stiffness…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-stryker-neurovascular-z-1740-2024

MLA

"Stryker Neurovascular — Class II recall: The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness…." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-stryker-neurovascular-z-1740-2024.

Chicago

Argus HQ Research. "Stryker Neurovascular — Class II recall: The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-stryker-neurovascular-z-1740-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_stryker_neurovascular_z_1740_2024_2024,
  title = {Stryker Neurovascular — Class II recall: The Distal Access Catheter is a single-lumen, braided shaft, variable stiffness…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-stryker-neurovascular-z-1740-2024},
  note = {Accessed: July 23, 2026}
}

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