Name: FDA Enforcement Actions Against AVID Medical, Inc.
Creator: Argus HQ
License: https://argushq.ai/methodology

AVID Medical, Inc. is a custom procedure-kit assembler whose Argus HQ tracked record consists of 14 device recalls across two distinct FDA report dates on Halyard-branded catheterization and OR kits. The May 13, 2026 event was a Class I recall wave across 10 Halyard cardiac cath, angiography, and neuro IR kits triggered by a supplier (Medline) syringe rotating-adaptor unwinding defect. The June 17, 2026 event was a Class II recall on 4 Halyard pain / eye / drape / towel packs from inadvertent distribution of sealed pouches that had not undergone validated sterilization. The tables below compute severity mix and reason patterns directly from those tracked records, each row linked to its FDA.gov source.

FDA action counts (Argus HQ database)

Total tracked FDA actions	14
Recalls	14
Warning letters	0
Form 483 inspection citations	0
Most recent tracked action	June 17, 2026
Most severe rating on file	critical

Recall severity breakdown

Computed from all 14 tracked recalls. FDA classifies each recall Class I (most serious), II, or III on the underlying record; Argus HQ maps that to critical/high/medium/low severity buckets.

critical	10 (71.4%)
high	4 (28.6%)

Recall velocity by month

Months with at least one tracked recall for AVID Medical, Inc., oldest to most recent. Gaps indicate months with zero tracked recalls, not missing data.

Month	Recalls
2026-05	10
2026-06	4

Recurring recall-reason patterns

Argus HQ keyword-matched the free-text “reason for recall” field on each tracked record into categories below. FDA does not publish a structured reason code for device recalls, so this is Argus HQ’s own pattern analysis, not an official FDA classification — records that don’t match a listed keyword fall into “Other.”

Other / not pattern-matched	10 recalls
Sterility	4 recalls

Full recall history (14)

Most recent first. Every row links to its Argus HQ record and FDA.gov source.

Date	Severity	Title
2026-06-17	high	AVID Medical, Inc. — Class II recall: Halyard, Pain Pack. Kit Code: AMPK48-01.
2026-06-17	high	AVID Medical, Inc. — Class II recall: Halyard, Drape Pack. Kit Code: LMDP36-01.
2026-06-17	high	AVID Medical, Inc. — Class II recall: Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
2026-06-17	high	AVID Medical, Inc. — Class II recall: Halyard, Towel Six Pack. Kit Code: AMTS70-01.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard CATH LAB kit. Model Number: SACL75-01.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
2026-05-13	critical	AVID Medical, Inc. — Class I recall: Halyard CATH LAB kit. Model Number: SACL75AM.

Coverage

No independent news coverage was found for AVID Medical, Inc.’s FDA recall history at the time this page was published — its enforcement record is small enough that it hasn’t drawn trade-press attention. This page is the most complete public record available.

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Full FDA history for AVID Medical, Inc.

Other enforcement deep dives

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Verified from FDA.gov · Last updated: Jun 17, 2026

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). AVID Medical, Inc.: FDA Enforcement History. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/enforcement/avid-medical-inc

MLA

"AVID Medical, Inc.: FDA Enforcement History." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/enforcement/avid-medical-inc.

Chicago

Argus HQ Research. "AVID Medical, Inc.: FDA Enforcement History." Digital Empire Holdings LLC. Accessed July 24, 2026. https://argushq.ai/enforcement/avid-medical-inc.

BibTeX

@misc{argushq_argushq_ai_enforcement_avid_medical_inc_2026,
  title = {AVID Medical, Inc.: FDA Enforcement History},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/enforcement/avid-medical-inc},
  note = {Accessed: July 24, 2026}
}

Source: FDA.gov (aggregated device recalls) ↗