AVID Medical, Inc. Recalls
16 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 →