Fresh Recalls

AVID Medical recalls

19 recent recalls on record for AVID Medical in connected official government data as of September 7, 2026 at 6:00 AM UTC.

Models with recalls

Halyard (4)Halyard CARDIAC CATH PACK SAN23CARDQ kit (1)Halyard CARDIAC CATH PACK kit (1)Halyard CARDIAC CATH TRAY SHANDS JAX kit (1)Halyard CATH LAB kit (2)Halyard EYE PACK (1)Halyard HEART CATH (1)Halyard NEURO IR PERIPHERAL (PS 64405) kit (1)Halyard PERC TRAY kit (1)Halyard SAMMC ANGIOGRAPHY kit (1)Halyard STANDARD LINE INSERTION PACK (1)Halyard VA DETROIT CATH LAB PACK kit (1)Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma (3)

All AVID Medical recalls

FDA Class I · Medical device · August 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.

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 Manifol…

Official ID Z-2798-2026 · Official record ↗

FDA Class I · Medical device · August 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.

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 Manifol…

Official ID Z-2797-2026 · Official record ↗

FDA Class I · Medical device · August 12, 2026

Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.

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 Manifol…

Official ID Z-2796-2026 · Official record ↗

FDA Class II · Medical device · July 29, 2026

Halyard STANDARD LINE INSERTION PACK recall — AVID Medical, Inc.

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.

Official ID Z-2772-2026 · Official record ↗

FDA Class II · Medical device · July 29, 2026

Halyard EYE PACK recall — AVID Medical, Inc.

Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

Official ID Z-2763-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Official ID Z-2410-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Official ID Z-2409-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Official ID Z-2408-2026 · Official record ↗

FDA Class II · Medical device · June 17, 2026

Halyard recall — AVID Medical, Inc.

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

Official ID Z-2407-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard VA DETROIT CATH LAB PACK kit recall — AVID Medical, Inc.

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.

Official ID Z-1979-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard SAMMC ANGIOGRAPHY kit recall — AVID Medical, Inc.

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.

Official ID Z-1978-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard PERC TRAY kit recall — AVID Medical, Inc.

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.

Official ID Z-1977-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard NEURO IR PERIPHERAL (PS 64405) kit recall — AVID Medical, Inc.

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.

Official ID Z-1976-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard HEART CATH recall — AVID Medical, Inc.

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.

Official ID Z-1975-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CATH LAB kit recall — AVID Medical, Inc.

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.

Official ID Z-1974-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CATH LAB kit recall — AVID Medical, Inc.

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.

Official ID Z-1973-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CARDIAC CATH TRAY SHANDS JAX kit recall — AVID Medical, Inc.

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.

Official ID Z-1972-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CARDIAC CATH PACK SAN23CARDQ kit recall — AVID Medical, Inc.

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.

Official ID Z-1971-2026 · Official record ↗

FDA Class I · Medical device · May 13, 2026

Halyard CARDIAC CATH PACK kit recall — AVID Medical, Inc.

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.

Official ID Z-1970-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.