AVID Medical Recalls
172 recalls on record · August 24, 2016 to August 12, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 12, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF
Hazard: 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.
August 12, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY
Hazard: 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.
August 12, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. CARDIAC CATH PACK
Hazard: 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.
July 29, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
Hazard: 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.
July 29, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Hazard: Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
June 17, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
Hazard: Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
June 17, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, Drape Pack. Kit Code: LMDP36-01.
Hazard: Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
June 17, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Hazard: Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
June 17, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, Pain Pack. Kit Code: AMPK48-01.
Hazard: Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard NEURO IR PERIPHERAL (PS 64405) kit. Model Number: UINR44-01.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard HEART CATH, SELF REGIONAL kit. Model Number: SELF131-05.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75-01.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CATH LAB kit. Model Number: SACL75AM.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Hazard: 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.
May 13, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05, WAFB208-02.
Hazard: 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.
February 18, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Hazard: Tyvek bag seal issue which may compromise sterility of the kit.
January 14, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
Hazard: Devices are not suitable for organ transplant.
January 14, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
Hazard: Devices are not suitable for organ transplant.
January 14, 2026Medical DevicesFDA
AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
Hazard: Devices are not suitable for organ transplant.
December 24, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, HEAD AND NECK TRAY. Catalog Number: EURO016-09.
Hazard: Potential for incomplete seal on header bag.
December 24, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, MAJOR PACK. Catalog Number: JEMJ10-01.
Hazard: Potential for incomplete seal on header bag.
December 24, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Hazard: Potential for incomplete seal on header bag.
December 24, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, EP LAB PK. Catalog Number: ESJH009-03.
Hazard: Potential for incomplete seal on header bag.
December 24, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.
Hazard: Potential for incomplete seal on header bag.
September 17, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit.
Hazard: Potential for open header bag seals, compromising sterility.
September 17, 2025Medical DevicesFDA
AVID Medical, Inc. recalls Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Hazard: Potential for open header bag seals, compromising sterility.