PlainRecalls

Avid Medical, Inc.

Compiled from official public sources by the editorial team.

163 recalls on record · Latest: May 13, 2026

Avid Medical, Inc. Recall Insight

Avid Medical, Inc. appears on 163 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.160% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 13, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 13 critical, 37 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Nov 20, 2024 to May 13, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Critical May 13, 2026

Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.

FDA Devices Critical May 13, 2026

Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.

FDA Devices Critical May 13, 2026

Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.

FDA Devices Critical May 13, 2026

Halyard CATH LAB kit. Model Number: SACL75-01.

FDA Devices Critical May 13, 2026

Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.

FDA Devices Critical May 13, 2026

Halyard CATH LAB kit. Model Number: SACL75AM.

FDA Devices Critical May 13, 2026

Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.

FDA Devices Critical May 13, 2026

Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.

FDA Devices Critical May 13, 2026

Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.

FDA Devices Critical May 13, 2026

Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.

FDA Devices Moderate Feb 18, 2026

Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.

FDA Devices Critical Jan 14, 2026

Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

FDA Devices Critical Jan 14, 2026

Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.

FDA Devices Critical Jan 14, 2026

Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

FDA Devices Moderate Dec 24, 2025

Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.

FDA Devices Moderate Dec 24, 2025

Halyard, EP LAB PK. Catalog Number: ESJH009-03.

FDA Devices Moderate Dec 24, 2025

Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.

FDA Devices Moderate Dec 24, 2025

Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.

FDA Devices Moderate Dec 24, 2025

Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.

FDA Devices Moderate Sep 17, 2025

Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.

FDA Devices Moderate Sep 17, 2025

Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit.

FDA Devices Moderate Aug 13, 2025

GYN ROBOTIC PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

LAP CHOLE PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

PACK GENERAL ROBOTIC. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

LAVH PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

LAPAROSCOPIC PROSTATECTOMY. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

LAPAROSCOPIC GYN. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

LAPAROSCOPIC TRAY. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

ROBOTIC URO/GYN PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

GYN LAPAROSCOPY PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

GENERAL LAPAROSCOPY TRAY. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

GEN LAPAROSCOPY PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

LAPAROSCOPY PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

MAJOR THORACOSCOPY BASIN. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

PARTIAL NEPHRECTOMY PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

HVI CARDIAC ROBOT PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

GENERAL ROBOTIC PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

CARDIAC ROBOT PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

DAVINCI UROLOGY. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

GS ENDOSCOPY PACK. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

CT DAVINCI. Medical convenience kit.

FDA Devices Moderate Aug 13, 2025

DA VINCI PACK URO/PROSTATE. Medical convenience kit.

FDA Devices Moderate May 21, 2025

Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit

FDA Devices Moderate May 21, 2025

Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.

FDA Devices Moderate May 21, 2025

Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.

FDA Devices Moderate Nov 20, 2024

Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06

FDA Devices Moderate Nov 20, 2024

Halyard PACEMAKER PACK - Medical convenience kits Model Number: MAMC223-08

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Avid Medical, Inc. with Zimmer Biomet, Inc. →

Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.