AVID Medical, Inc. Recalls
31 recalls on record in the United States
AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75-01.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WA
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75AM.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UI
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
View recall details →
AVID Medical, Inc. recalls Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
View recall details →
AVID Medical, Inc. recalls Halyard, Pain Pack. Kit Code: AMPK48-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
View recall details →
AVID Medical, Inc. recalls Halyard, Drape Pack. Kit Code: LMDP36-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
View recall details →
AVID Medical, Inc. recalls Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
View recall details →
AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number:
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.
View recall details →
AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenienc
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
View recall details →
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic A
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
View recall details →
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic A
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
View recall details →
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic A
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path has the potential to be introduced into blood circulation and become lodged within blood vessels.
View recall details →
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
View recall details →
AVID Medical, Inc. recalls Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containi
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
View recall details →
AVID Medical, Inc. recalls Halyard medical convenience kits labeled as: 1) A-P PACK
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
View recall details →
AVID Medical, Inc. recalls Halyard medical convenience kits labeled as: 1) ENT, Mode
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
View recall details →
AVID Medical, Inc. recalls 1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3)
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
View recall details →
Showing 30 of 31 recalls. See all →