AVID Medical, Inc. recalls
62 recalls.
- Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH30. recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 28, 2026 · A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. - Halyard ANTERIOR HIP PACK. Model/Catalog Number: SOAH31. recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 28, 2026 · A non-sterile component was piggybacked and incorrectly placed outside of the sterile barrier and not subjected to EO sterilization per kit specifications. - ABD HYSTERECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - MAJOR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - UROLOGY MAJOR recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - HEART PREP TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI LAP/GYN recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PLASTICS TRAY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - LAPAROSCOPIC PROSTATECTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ROBOTIC PROSTATECTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - PACK OPEN HEART CFH recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - CRANIOTOMY PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ENDOVASCULAR PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - ADULT HEART TRAY SHANDS JACKS recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - GYN LAPAROSCOPY/LAPAROTOMY recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - DAVINCI TRUCUSTOM BUNDLE recall (AVID Medical, Inc.)
Medical deviceClass IIReported October 14, 2026 · Product may be potentially contaminated with a lubricant used during the manufacturing process. - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator. - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator. - Halyard IV START KIT NON-STERILE recall (AVID Medical, Inc.)
Medical deviceClass IReported September 30, 2026 · Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides. - Haylard UNIV IMAGING BIOPSY TRUCUSTOM recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Haylard BASIC BIOPSY TRAY recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Haylard CONTINUOUS NERVE BLOCK TRAY recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Haylard 18G SINGLE SHOT EPI TRAY recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Halyard IV START KIT NON-STERILE REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IReported September 23, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides - Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 16, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper... - Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - 1) NEURO recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Halyard medical convenience kits labeled as: 1) ENT recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY... recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard LAVH PACK recall (AVID Medical, Inc.)
Medical deviceClass IIReported August 26, 2026 · The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit. - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard convenience kits containing recalled Medline Namic Angiographic Star Off... recall (AVID Medical, Inc.)
Medical deviceClass IReported August 12, 2026 · Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within... - Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. ... recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. - Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit. recall (AVID Medical, Inc.)
Medical deviceClass IIReported July 29, 2026 · Incorrect concentration of Betadine solution contained within certain AVID convenience kits. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Inadvertent distribution of sealed pouches that had not undergone validated sterilization. - Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard PERC TRAY kit. Model Numbers: SLPC34-01 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard NEURO IR PERIPHERAL recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard HEART CATH recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75-01. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75AM. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01. recall (AVID Medical, Inc.)
Medical deviceClass IIReported February 18, 2026 · Tyvek bag seal issue which may compromise sterility of the kit. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag. - Halyard recall (AVID Medical, Inc.)
Medical deviceClass IIReported December 24, 2025 · Potential for incomplete seal on header bag.