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 |
|---|---|---|---|
| Aug 10, 2026 | PLASTICS TRAY; Model/Item Number (Kit): EURO053; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | HEART PREP TRAY; Model/Item Number (Kit): MECV97W; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | PACK OPEN HEART CFH; Model/Item Number (Kit): 1. UFCF004-06, 2. UFCF004-07; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | LAPAROSCOPIC PROSTATECTOMY; Model/Item Number (Kit): NIHB0036-07; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | MAJOR PACK; Model/Item Number (Kit): NIHB0018-11; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | GYN LAPAROSCOPY/LAPAROTOMY; Model/Item Number (Kit): 1. WRNM002-15, 2. FBCH1... | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | ABD HYSTERECTOMY; Model/Item Number (Kit): NAMC438-07; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | GYN LAPAROSCOPY PACK; Model/Item Number (Kit): NAMC436-12; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | DAVINCI TRUCUSTOM BUNDLE; Model/Item Number (Kit): 1. SAMM064-27, 2. SAMM064... | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | UROLOGY MAJOR; Model/Item Number (Kit): WRNM058-10; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | CRANIOTOMY PACK; Model/Item Number (Kit): WRNM035-20; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | ADULT HEART TRAY SHANDS JACKS; Model/Item Number (Kit): SHND419-08; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11; | Product may be potentially contaminated with a lubricant used during the manu... | Class II |
| Aug 10, 2026 | Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05; | Potential for product quality and sterility issues regarding kits containing ... | Class I |
| Aug 10, 2026 | Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415; | Potential for product quality and sterility issues regarding kits containing ... | Class I |
| Aug 10, 2026 | Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03; | Potential for product quality and sterility issues regarding kits containing ... | Class I |
| Aug 10, 2026 | Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02; | Potential for product quality and sterility issues regarding kits containing ... | Class I |
| Jul 22, 2026 | Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep ... | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may ... | Class II |
| Jul 22, 2026 | Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep ... | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may ... | Class II |
| Jul 22, 2026 | Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep ... | Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may ... | Class I |
| Jul 14, 2026 | Halyard IV START KIT NON-STERILE REF: KRIV26-02 | Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Ap... | Class I |
| Jul 14, 2026 | Halyard IV Start Kit Non-Sterile REF: KRIV26-02 | Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL A... | Class II |
| 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 | 1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKC... | The recall notice was initiated due to a Medicom Urgent Medical Device Recall... | Class II |
| May 19, 2026 | Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (ki... | The recall notice was initiated due to a Medicom Urgent Medical Device Recall... | Class II |
| May 19, 2026 | Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/I... | The recall notice was initiated due to a Medicom Urgent Medical Device Recall... | 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 |
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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