Has Abbott Medical had other FDA enforcement actions?

Yes. Argus HQ has recorded 39 total FDA actions tied to Abbott Medical: 0 warning letters, 39 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 2024-07-10; 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

Abbott Medical — Class II recall: Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY

Name: FDA Recall Record — Abbott Medical
Creator: Argus HQ
Published: 2024-07-10
License: https://argushq.ai/methodology

Event date: 2024-07-10 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-2265-2024
Payload hash: 11384412957a529769a60df0…

Summary

Deep brain stimulation system will first turn off after approximately 50 days after the system is activated and subsequently, this same action will recur approximately every 50 days thereafter. This unexpected lost of stimulation may result in loss of therapy. Status: Ongoing.

Entities

Abbott Medical

View source record ↗

Frequently asked questions

Has Abbott Medical had other FDA enforcement actions?: Yes. Argus HQ has recorded 39 total FDA actions tied to Abbott Medical: 0 warning letters, 39 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 2024-07-10; 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). Abbott Medical — Class II recall: Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-abbott-medical-z-2265-2024

MLA

"Abbott Medical — Class II recall: Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-abbott-medical-z-2265-2024.

Chicago

Argus HQ Research. "Abbott Medical — Class II recall: Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-abbott-medical-z-2265-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_abbott_medical_z_2265_2024_2024,
  title = {Abbott Medical — Class II recall: Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-abbott-medical-z-2265-2024},
  note = {Accessed: July 23, 2026}
}

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