AVID Medical, Inc.

Complete recall history across all FDA and CPSC categories, 153 total recalls

AVID Medical, Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (153)

FDA medical device enforcement actions by AVID Medical, Inc.. Showing most recent 50.

Date Product Reason Class
Jul 10, 2026 Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visua... The kit component was subjected to EO sterilization, contrary to the manufact... Class II
Jul 9, 2026 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
Jul 9, 2026 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
Jul 9, 2026 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
Jul 9, 2026 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
Jul 9, 2026 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
Jul 9, 2026 Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY ... Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
Jul 9, 2026 Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 Labeling Deficiency: The medical kit labeling fails to identify that the stat... Class II
May 19, 2026 Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. C... Defects in the silicone seal, which may result in "doming" of the silicone se... Class II
May 7, 2026 Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. Incorrect concentration of Betadine solution contained within certain AVID co... Class II
Apr 30, 2026 Halyard convenience kits containing recalled Medline Namic Angiographic Star ... Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, w... Class I
Apr 30, 2026 Halyard convenience kits containing recalled Medline Namic Angiographic Star ... Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, w... Class I
Apr 30, 2026 Halyard convenience kits containing recalled Medline Namic Angiographic Star ... Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, w... Class I
Apr 30, 2026 Halyard, Eye Bag Pack. Kit Code: UIEB48-01. Inadvertent distribution of sealed pouches that had not undergone validated s... Class II
Apr 30, 2026 Halyard, Drape Pack. Kit Code: LMDP36-01. Inadvertent distribution of sealed pouches that had not undergone validated s... Class II
Apr 30, 2026 Halyard, Pain Pack. Kit Code: AMPK48-01. Inadvertent distribution of sealed pouches that had not undergone validated s... Class II
Apr 30, 2026 Halyard, Towel Six Pack. Kit Code: AMTS70-01. Inadvertent distribution of sealed pouches that had not undergone validated s... Class II
Mar 13, 2026 Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard CATH LAB kit. Model Number: SACL75AM. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard CATH LAB kit. Model Number: SACL75-01. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Mar 13, 2026 Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05. Potential risk for Medline syringe rotating adaptor unwinding during use, whi... Class I
Jan 2, 2026 Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. Tyvek bag seal issue which may compromise sterility of the kit. Class II
Nov 14, 2025 Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10. Potential for incomplete seal on header bag. Class II
Nov 14, 2025 Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09. Potential for incomplete seal on header bag. Class II
Nov 14, 2025 Halyard, MAJOR PACK. Catalog Number: JEMJ10-01. Potential for incomplete seal on header bag. Class II
Nov 14, 2025 Halyard, EP LAB PK. Catalog Number: ESJH009-03. Potential for incomplete seal on header bag. Class II
Nov 14, 2025 Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01. Potential for incomplete seal on header bag. Class II
Nov 11, 2025 Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08 Devices are not suitable for organ transplant. Class I
Nov 11, 2025 Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15. Devices are not suitable for organ transplant. Class I
Nov 11, 2025 Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17. Devices are not suitable for organ transplant. Class I
Aug 4, 2025 Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit. Potential for open header bag seals, compromising sterility. Class II
Aug 4, 2025 Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit. Potential for open header bag seals, compromising sterility. Class II
Jun 11, 2025 DA VINCI PACK URO/PROSTATE. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 CT DAVINCI. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 GS ENDOSCOPY PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 DAVINCI UROLOGY. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 CARDIAC ROBOT PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 GENERAL ROBOTIC PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 HVI CARDIAC ROBOT PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 PARTIAL NEPHRECTOMY PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 MAJOR THORACOSCOPY BASIN. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 LAPAROSCOPY PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 GEN LAPAROSCOPY PACK. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II
Jun 11, 2025 GENERAL LAPAROSCOPY TRAY. Medical convenience kit. CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing... Class II

View all 153 device recalls →

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious, there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious, the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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