Has AVID Medical, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 30 total FDA actions tied to AVID Medical, Inc.: 0 warning letters, 30 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 2026-09-09; Argus observed and indexed it on 2026-09-15.

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

AVID Medical, Inc. — Class II recall: Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item…

Name: FDA Recall Record — AVID Medical, Inc.
Creator: Argus HQ
Published: 2026-09-09
License: https://argushq.ai/methodology

Event date: 2026-09-09 00:00:00Z
Observed: 2026-09-15 04:20:26Z
Source ID: Z-3046-2026
Payload hash: f740695a3c4ef2c3d7d264d7…

Summary

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products. Status: Ongoing.

Entities

AVID Medical, Inc.

View source record ↗

Frequently asked questions

Has AVID Medical, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 30 total FDA actions tied to AVID Medical, Inc.: 0 warning letters, 30 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 2026-09-09; Argus observed and indexed it on 2026-09-15.
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). AVID Medical, Inc. — Class II recall: Halyard medical convenience kits labeled as:    1) A-P PACK - 205936, Model/Item…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-avid-medical-inc-z-3046-2026

MLA

"AVID Medical, Inc. — Class II recall: Halyard medical convenience kits labeled as:    1) A-P PACK - 205936, Model/Item…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-avid-medical-inc-z-3046-2026.

Chicago

Argus HQ Research. "AVID Medical, Inc. — Class II recall: Halyard medical convenience kits labeled as:    1) A-P PACK - 205936, Model/Item…." Digital Empire Holdings LLC. Accessed September 15, 2026. https://argushq.ai/events/fda-recall-avid-medical-inc-z-3046-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_avid_medical_inc_z_3046_2026_2026,
  title = {AVID Medical, Inc. — Class II recall: Halyard medical convenience kits labeled as:    1) A-P PACK - 205936, Model/Item…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-avid-medical-inc-z-3046-2026},
  note = {Accessed: September 15, 2026}
}

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