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fda_recall · device_recall · high

Medtronic Inc — Class II recall: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090 AB9G1210009…

Event date
2026-01-21 00:00:00Z
Observed
2026-07-16 23:20:07Z
Source ID
Z-1098-2026
Payload hash
d8e85b15c5a748f12da08439

Summary

Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force. Issue may result in stent migration. Status: Ongoing.

Frequently asked questions

Has Medtronic, Inc. had other FDA enforcement actions?
Yes. Argus HQ has recorded 40 total FDA actions tied to Medtronic, Inc.: 0 warning letters, 40 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 2026-01-21; 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 (2026). Medtronic Inc — Class II recall: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090  AB9G1210009…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-medtronic-inc-z-1098-2026
MLA
"Medtronic Inc — Class II recall: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090  AB9G1210009…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-medtronic-inc-z-1098-2026.
Chicago
Argus HQ Research. "Medtronic Inc — Class II recall: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090  AB9G1210009…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-medtronic-inc-z-1098-2026.
BibTeX
@misc{argushq_argushq_ai_events_fda_recall_medtronic_inc_z_1098_2026_2026,
  title = {Medtronic Inc — Class II recall: Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090  AB9G1210009…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-medtronic-inc-z-1098-2026},
  note = {Accessed: July 23, 2026}
}

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