PlainRecalls

Avid Medical, Inc.

Compiled from official public sources by the publisher.

172 recalls on record · Latest: Aug 12, 2026

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Agency notice ledger

Federal filing book Avid Medical, Inc. HEAVY-BOOK · SINGLE-AGENCY

#91 of 14,151 · 172 notices · 0.165% archive

  • BOOK 172 notices
  • RANK #91 of 14,151
  • SHARE 0.165% archive
  • AGENCY FDA Devices (172)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 12, 2026
  • PHOTO CareFusion 303, Inc.

Nearest notice-volume peer: CareFusion 303, Inc. (1 notice gap)

Avid Medical, Inc. accounts for about 0.165% of the 104,423-notice archive on 172 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Avid Medical, Inc.'s standing among 14,151 recalling firms

Avid Medical, Inc. ranks 91st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Avid Medical, Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

172 91st of 14151 higher than 14,060 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Avid Medical, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Avid Medical, Inc. holds about 0.165% of archive notices alongside 172 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Critical Aug 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
FDA Devices Critical Aug 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK EAMC1000-05
FDA Devices Critical Aug 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF REGIONAL SELF131-05
FDA Devices Moderate Jul 29, 2026

Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
FDA Devices Moderate Jul 29, 2026

Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
FDA Devices Moderate Jun 17, 2026

Halyard, Towel Six Pack. Kit Code: AMTS70-01.
FDA Devices Moderate Jun 17, 2026

Halyard, Pain Pack. Kit Code: AMPK48-01.
FDA Devices Moderate Jun 17, 2026

Halyard, Drape Pack. Kit Code: LMDP36-01.
FDA Devices Moderate Jun 17, 2026

Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
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.

Avid Medical, Inc. carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

CareFusion 303, Inc. 173 Ge Medical Systems, LLC 168 Fresenius Medical Care Holdings, Inc. 166 Becton Dickinson & Company 179

Frequently Asked Questions

How many federal recall notices name Avid Medical, Inc.? ▼
PlainRecalls indexes 172 distinct federal recall events naming Avid Medical, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Avid Medical, Inc. sit among other recalling firms? ▼
Avid Medical, Inc. ranks #91 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Avid Medical, Inc.'s notices? ▼
FDA Devices accounts for 172 of this firm's 172 indexed notices.
What product category dominates Avid Medical, Inc.'s filing book? ▼
Filings for Avid Medical, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Avid Medical, Inc.: 172 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Avid Medical, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026